Drug target isogenes: polymorphisms in the Interleukin 4 Receptor Alpha gene

ABSTRACT

Polynucleotides comprising one or more of 38 novel single nucleotide polymorphisms in the human Interleukin 4 Receptor Alpha(IL4Rα) gene are described. Compositions and methods for detecting one or more of these polymorphisms are also disclosed. In addition, various genotypes and haplotypes for IL4Rα gene that exist in the population are described.

RELATED APPLICATIONS

[0001] This application is a division of PCT/US00/19094, filed Jul. 13, 2000.

FIELD OF THE INVENTION

[0002] This invention relates to variation in genes that encode pharmaceutically important proteins. In particular, this invention provides genetic variants of the human Interleukin 4 Receptor Alpha (IL4Rα) gene and methods for identifying which variant(s) of this gene is/are possessed by an individual.

BACKGROUND OF THE INVENTION

[0003] Current methods for identifying pharmaceuticals to treat disease often start by identifying, cloning, and expressing an important target protein related to the disease. A determination of whether an agonist or antagonist is needed to produce an effect that may benefit a patient with the disease is then made. Then, vast numbers of compounds are screened against the target protein to find new potential drugs. The desired outcome of this process is a drug that is specific for the target, thereby reducing the incidence of the undesired side effects usually caused by a compound's activity at non-intended targets.

[0004] What this approach fails to consider, however, is that natural variability exists in any and every population with respect to a particular protein. A target protein currently used to screen drugs typically is expressed by a gene cloned from an individual who was arbitrarily selected. However, the nucleotide sequence of a particular gene may vary tremendously among individuals. Subtle alteration(s) in the primary nucleotide sequence of a gene encoding a target protein may be manifested as significant variation in expression of or in the structure and/or function of the protein. Such alterations may explain the relatively high degree of uncertainty inherent in treatment of individuals with drugs whose design is based upon a single representative example of the target. For example, it is well-established that some classes of drugs frequently have lower efficacy in some individuals than others, which means such individuals and their physicians must weigh the possible benefit of a larger dosage against a greater risk of side effects. In addition, variable information on the biological function or effects of a particular protein may be due to different scientists unknowingly studying different isoforms of the gene encoding the protein. Thus, information on the type and frequency of genomic variation that exists for pharmaceutically important proteins would be useful.

[0005] The organization of single nucleotide variations (polymorphisms) in the primary sequence of a gene into one of the limited number of combinations that exist as units of inheritance is termed a haplotype. Each haplotype therefore contains significantly more information than individual unorganized polymorphisms. Haplotypes provide an accurate measurement of the genomic variation in the two chromosomes of an individual.

[0006] It is well-established that many diseases are associated with specific variations in gene sequences. However while there are examples in which individual polymorphisms act as genetic markers for a particular phenotype, in other cases an individual polymorphism may be found in a variety of genomic backgrounds and therefore shows no definitive coupling between the polymorphism and the causative site for the phenotype (Clark A G et al. 1998 Am J Hum Genet 63:595-612; Ulbrecht M et al. 2000 Am J Respir Crit Care Med 161: 469-74). In addition, the marker may be predictive in some populations, but not in other populations (Clark A G et al. 1998 supra). In these instances, a haplotype will provide a superior genetic marker for the phenotype (Clark A G et al. 1998 supra; Ulbrecht M et al. 2000, supra; Ruaño G & Stephens J C Gen Eng News 19 (21), December 1999).

[0007] Analysis of the association between each observed haplotype and a particular phenotype permits ranking of each haplotype by its statistical power of prediction for the phenotype. Haplotypes found to be strongly associated with the phenotype can then have that positive association confirmed by alternative methods to minimize false positives. For a gene suspected to be associated with a particular phenotype, if no observed haplotypes for that gene show association with the phenotype of interest, then it may be inferred that variation in the gene has little, if any, involvement with that phenotype (Ruano & Stephens 1999, supra). Thus, information on the observed haplotypes and their frequency of occurrence in various population groups will be useful in a variety of research and clinical applications.

[0008] One possible drug target for the treatment of allergies, asthma, and other immune responses is the Interleukin 4 Receptor Alpha (IL4Rα) gene or its encoded product. IL4R is a transmembrane complex composed of two different protein subunits, a 140-kDa high affinity binding subunit named interleukin-4 receptor a (IL-4Rα; also known as CD 124 antigen) and either a gamma-c subunit, which is present in several cytokine receptors, or an interleukin- 13 receptor 1 (IL- 1 3R1) subunit. Both subunits of the IL-4R are required to bind interleukin-4 (IL-4) and to mediate its transcription-activating effects through the tyrosine kinases, Jak1 and Jak3. Upon binding of IL-4 to the IL-4R, Jak 1 and Jak 3 phosphorylate the IL-4Rα subunit, creating binding sites in the cytoplasmic domain for many other proteins, including SOS, Stat-6, c-fes, and src homology phosphatase 1 (SHP-1). Activated Jak proteins also phosphorylate Stat-proteins, which travel into the nucleus and function as transcription factors. Other IL-4 signal pathways exist, but are less well characterized.

[0009] IL-4, one of the most important cytokines involved in the allergic response, is produced when cells from the immune system, in particular T cells, are activated in response to an allergen. Regulation of the immune response involves Helper T-cells that differentiate into two subtypes, Th1 and Th2. Th1 cells express interferon-gamma and interluekin-2 (IL-2), and mediate a cell-based immunity, where macrophages and neutrophils are prominently involved. Th1 cells also direct the IgE-producing B cells, as well as mast cells, basophils and eosinophils. Th2 cells produce IL-4, IL-5, IL-6, IL-10 and IL-13. Each Th cell subtype represses the other, so the immune system is forced into differentiation into either a Th1 or Th2 response against an external allergic challenge. In many instances an aberration of this response can render a pathological state such as a Th2 response against. ragweed.

[0010] IL-4 induces in B cells the synthesis of IgE type antibodies that recognize specific allergens. IgE binds to receptors on mast cells and basophils and mediates the early humoral (sub-chronic) response on the B-side of the immune system. If an allergen binds mast cell-attached IgE, the mast cell releases mediators like histamine, and the eicosanoid leukotrienes and prostaglandins products, some of which cause the familiar symptoms of an acute allergic reaction: swelling, itching, mucous, and reddening of the skin. Later in this process eosinophils and other inflammatory cells migrate to the site of inflammation. This later phase is important in asthma, because the eosinophils may instigate a more chronic inflammation which can adversely scar lung tissue. IL-4 is at least partly responsible for recruiting eosinophils, because it induces synthesis of specific adhesion molecules on the capillary endothelium, and stimulates expression of IL-5 and eotaxin. IL-5 leads to the development of a large number of eosinophils from precursor cells in the bone marrow, and eotaxin stimulates their migration into the lung tissue.

[0011] It has been proposed that inhibition of IL-4 activity would disarm the Th2 component of the immune system. This would then allow the immune system to develop a natural tolerance towards common allergens without the full acute response to the challenge. In this way, tolerance may be induced in many patients, similar to what is sometimes achieved with hyposensitization shots for allergy patients. Thus, substances that inhibit IL-4 production and/or its binding to the IL-4 receptor, may improve the therapy of allergies and asthma.

[0012] The gene for IL-4Rα has eleven exons encoding an 825 amino acid protein and spans over 24 kb of the short arm of chromosome 16 (16p 12.1) (Pritchard et al., Genomics 10:801, 1991; GenBank Accession No. AC004525). A reference sequence for IL4R-α gene, which corresponds to the reverse complement of nucleotides 100020-71331 in the GenBank Accession No. AC004525, is shown in FIG. 1 (SEQ ID NO:1). Reference sequences for IL-4Rα mRNA (GenBank Accession No. NM_(—)000418) and the encoded IL4Rα precursor protein (GenBank Accession No. P24394) are shown in FIGS. 2 and 3, respectively (SEQ ID NOS:2 and 3). Significant features reported for the IL-4Rα precursor include: a signal peptide located between a.a. 1 and 25; an extracellular domain between a.a. 26 and 232; disulfide bonds between a.a. 34 and 44 and between a.a. 74 and 86; glycosylation sites at amino acids 53, 98, 128, 134, 176, and 209; a transmembrane region between a.a. 233 and 256; and a cytoplasmic domain between a.a. 257 and 825.

[0013] Recently, several studies have suggested that genetic polymorphisms in the IL-4-Rα gene are associated with genetic predisposition to atopy and/or elevated serum IgE. Mitsuyasu et al., reported that polymorphisms at codons 75 and 576 affect IL-4R function (Nat. Genet. 19:119-120, 1998). The IL-4Rα allele with isoleucine at amino acid position 75 (Ile75) in the extracellular domain is more responsive to IL-4 than the allele with valine at that position (Val75) and is associated with atopic asthma but not with non-atopic asthma (Mitsuyasu et al., supra). Also, the allele with arginine at position 576 (Arg576) in the cytoplasmic domain exhibits higher receptor activity than the glutamine allele (Glu576) due to reduced binding by the Arg576 allele of a negative regulatory molecule, src homology phosphatase 1 (Imani et al., J. Biol Chem. 272:7927-7931, 1997). The Arg576 allele has a higher frequency in patients with allergic inflammatory disorders, including atopy (Khurana Hershey et al., New Eng. J. Med. 337:1720-1725, 1997). In a recent study, Hershey et al., (WO 00/34789) reported that the-Arg576 allele is significantly associated with asthma. Studies showed that patients who were homozygous for this allele had about a 9-fold higher risk towards asthma and that two copies of Arg576 are associated in an increase in asthma prevalence and severity. Kanemitsu et al. recently reported that the presence of either the Ile75 or Arg576 variant is significantly associated with susceptibility for developing systemic lupus erythematosus (SLE), a Th2-dominant systemic autoinumune disorder (Arthritis Rheum. 42:1298-1300). Another variant IL-4Rα allele that is reportedly associated with atopy susceptibility has proline rather than serine at position 503 (Kruse et al., Immunol. 96:365-371, 1999). Other IL-4Rα gene polymorphisms leading to amino acid changes in the cytoplasmic domain of the protein product have been identified at codons 400 (E400A), 431 (C431R) and 786 (S786P) (Kruse et al., supra; Deichmann et al., Biochem. Biophys. Res. Commun. 231:696-697, 1997). A polymorphism of guanine or adenine at a position corresponding to nucleotide 55328 in FIG. 1 has also been reported as well as a polymorphism of cytosine or thymine at a position corresponding to nucleotide 55430 (Buetow et al., 1999, Nat Genet. 21:323-5).

[0014] Because of the potential for polymorphisms in the IL4Rα gene to affect the expression and function of the encoded protein, it would be useful to determine whether additional polymorphisms exist in the IL4Rα gene, as well as how such polymorphisms are combined in different copies of the gene. Such information would be useful for studying the biological function of IL4Rα as well as in identifying drugs targeting this protein for the treatment of disorders related to its abnormal expression or function.

SUMMARY OF THE INVENTION

[0015] Accordingly, the inventors herein have discovered 38 novel polymorphic sites in the IL4Rα gene. These polymorphic sites (PS) correspond to the following nucleotide positions in the reverse complement of the indicated GenBank Accession Number: 32884 (PS1), 32903 (PS2), 32961 (PS3), 33135 (PS4), 35763 (PS6), 35770 (PS7), 35817 (PS8), 35905 (PS9), 35944 (PS10), 35958 (PS11), 37330 (PS12), 37473 (PS13), 37586 (PS14), 37591 (PS15), 37604 (PS16), 37644 (PS17), 37678 (PS18), 43446 (PS19), 43703 (PS20), 53008 (PS21), 53099 (PS22), 53153 (PS23), 53456 (PS25), 53507 (PS27), 53513 (PS28), 53915 (PS30), 53949 (PS32), 54237 (PS33), 54468 (PS34), 54611 (PS35), 54698 (PS36), 54700 (PS37), 54741 (PS38), 54780 (PS39), 55083 (PS40), 55142 (PS41), 55539 (PS44) and 55758 (PS45) in AC004525. The polymorphisms at these sites are adenine or guanine at PS1, cytosine or thymine at PS2, guanine or thymine at PS3, guanine or cytosine at PS4, cytosine or thymine at PS6, guanine or adenine at PS7, thymine or cytosine at PS8, cytosine or thymine at PS9, cytosine or thymine at PS10, guanine or adenine at PS11, guanine or adenine at PS12, cytosine or thymine at PS13, cytosine or thymine at PS14, guanine or adenine at PS15, adenine or thymine at PS16, cytosine or adenine at PS17, cytosine or thymine at PS18, guanine or adenine at PS19, thymine or cytosine at PS20, adenine or cytosine at PS21, cytosine or thymine at PS22, thymine or cytosine at PS23, guanine or thymine at PS25, cytosine or thymine at PS27, thymine or cytosine at PS28, cytosine or thymine at PS30, guanine or adenine at PS32, cytosine or thymine at PS33, thymine or guanine at PS34, thymine or cytosine at PS35, thymine or cytosine at PS36, thymine or cytosine at PS37, cytosine or thymine at PS38, cytosine or guanine at PS39, adenine or guanine at PS40, guanine or adenine at PS41, cytosine or thymine at PS44 and guanine or adenine at PS45. In addition, the inventors have determined the identity of the alternative nucleotides present at these sites, as well as at the previously identified sites at nucleotides 35749 (PS5), 53413 (PS24), 53505 (PS26), 53721 (PS29), 53941 (PS31), 55328 (PS42), and 55430 (PS43). It is believed that IL4Rα-encoding polynucleotides containing one or more of the novel polymorphic sites reported herein will be useful in studying the expression and biological function of IL4α, as well as in developing drugs targeting this protein. In addition, information on the combinations of polymorphisms in the IL4Rα gene may have diagnostic and forensic applications.

[0016] Thus, in one embodiment, the invention provides an isolated polynucleotide comprising a nucleotide sequence which is a polymorphic variant of a reference sequence for the IL4Rα gene or a fragment thereof. The reference sequence comprises SEQ ID NO:1 and the polymorphic variant comprises at least one polymorphism selected from the group consisting of guanine at PS1, thymine at PS2, thymine at PS3, cytosine at PS4, thymine at PS6, adenine at PS7, cytosine at PS8, thymine at PS9, thymine at PS10, adenine at PS11, adenine at PS12, thymine at PS13, thymine at PS14, adenine at PS15, thymine at PS16, adenine at PS17, thymine at PS18, adenine at PS19, cytosine at PS20, cytosine at PS21, thymine at PS22, cytosine at PS23, thymine at PS25, thymine at PS27, cytosine at PS28, thymine at PS30, adenine at PS32, thymine at PS33, guanine at PS34, cytosine at PS35, cytosine at PS36, cytosine at PS37, thymine at PS38, guanine at PS39, guanine at PS40, adenine at PS41, thymine at PS44, and adenine at PS45. In a preferred embodiment, the polymorphic variant comprises one or more additional polymorphisms selected from the group consisting of guanine at PS5, cytosine at PS24, cytosine at PS26, cytosine at PS29, guanine at PS31, adenine at PS42, and thymine at PS43. A particularly preferred polymorphic variant is a naturally-occurring isoform (also referred to herein as an “isogene”) of the IL4Rα gene. An IL4Rα isogene of the invention comprises adenine or guanine at PS1, cytosine or thymine at PS2, guanine or thymine at PS3, guanine or cytosine at PS4, cytosine or thymine at PS6, guanine or adenine at PS7, thymine or cytosine at PS8, cytosine or thymine at PS9, cytosine or thymine at PS10, guanine or adenine at PS11, guanine or adenine at PS12, cytosine or thymine at PS13, cytosine or thymine at PS14, guanine or adenine at PS15, adenine or thymine at PS16, cytosine or adenine at PS17, cytosine or thymine at PS18, guanine or adenine at PS19, thymine or cytosine at PS20, adenine or cytosine at PS21, cytosine or thymine at PS22, thymine or cytosine at PS23, guanine or thymine at PS25, cytosine or thymine at PS27, thymine or cytosine at PS28, cytosine or thymine at PS30, guanine or adenine at PS32, cytosine or thymine at PS33, thymine or guanine at PS34, thymine or cytosine at PS35, thymine or cytosine at PS36, thymine or cytosine at PS37, cytosine or thymine at PS38, cytosine or guanine at PS39, adenine or guanine at PS40, guanine or adenine at PS41, cytosine or thymine at PS44 and guanine or adenine at PS45. The invention also provides a collection of IL4Rα isogenes, referred to herein as an IL4Rα genome anthology.

[0017] An IL4Rα isogene may be defined by the combination and order of these polymorphisms in the isogene, which is referred to herein as an IL4Rα haplotype. Thus, the invention also provides data on the number of different IL4Rα haplotypes found in the above four population groups. This haplotype data is useful in methods for deriving an IL4Rα haplotype from an individual's genotype for the IL4Rα gene and for determining an association between an IL4Rα haplotype and a particular trait.

[0018] In another embodiment, the invention provides a polynucleotide comprising a polymorphic variant of a reference sequence for an IL4Rα cDNA or a fragment thereof. The reference sequence comprises SEQ ID NO:2 (FIG. 2) and the polymorphic cDNA comprises at least one polymorphism selected from the group consisting of thymine at a position corresponding to nucleotide 237, adenine at a position corresponding to nucleotide 244, cytosine at a position corresponding to nucleotide 291, thymine at a position corresponding to nucleotide 501, adenine at a position corresponding to nucleotide 554, cytosine at a position corresponding to nucleotide 939, thymine at a position corresponding to nucleotide 1242, thymine at a position corresponding to nucleotide 1293, cytosine at a position corresponding to nucleotide 1299, thymine at a position corresponding to nucleotide 1701, adenine at a position corresponding to nucleotide 1735, thymine at a position corresponding to nucleotide 2023, guanine at a position corresponding to nucleotide 2254 and cytosine at a position corresponding to nucleotide 2397. In a preferred embodiment, the polymorphic variant comprises one or more additional polymorphisms selected from the group consisting of guanine at a position corresponding to 223, cytosine at a position corresponding to nucleotide 1199, cytosine at a position corresponding to 1291, cytosine at a position corresponding to nucleotide 1507 and guanine at a position corresponding to 1737.

[0019] Polynucleotides complementary to these IL4Rα genomic and cDNA variants are also provided by the invention.

[0020] In other embodiments, the invention provides a recombinant expression vector comprising one of the polymorphic genomic variants operably linked to expression regulatory elements as well as a recombinant host cell transformed or transfected with the expression vector. The recombinant vector and host cell may be used to express IL4Rα for protein structure analysis and drug binding studies.

[0021] In yet another embodiment, the invention provides a polypeptide comprising a polymorphic variant of a reference amino acid sequence for the IL4Rα protein. The reference amino acid sequence comprises SEQ ID NO:3 (FIG. 3) and the polymorphic variant comprises at least one variant amino acid selected from the group consisting of threonine at a position corresponding to amino acid 82, histidine at a position corresponding to amino acid 185, isoleucine at a position corresponding to amino acid 579, serine at a position corresponding to amino acid 675, and alanine at a position corresponding to amino acid 752. In some embodiments, the polymorphic variant also comprises at least one variant amino acid selected from the group consisting of valine at a position corresponding to amino acid 75, alanine at a position corresponding to amino acid 400, arginine at a position correpsonding to amino acid 431, proline at a position corresponding to amino acid 503, and arginine at a position corresponding to amino acid 576. A polymorphic variant of IL4Rα is useful in studying the effect of the variation on the biological activity of IL4Rα as well as studying the binding affinity of candidate drugs targeting IL4Rα for the treatment of allergies, asthma, and other immune responses.

[0022] The present invention also provides antibodies that recognize and bind to the above polymorphic IL4Rα protein variant. Such antibodies can be utilized in a variety of diagnostic and prognostic formats and therapeutic methods.

[0023] In other embodiments, the invention provides methods, compositions, and kits for haplotyping and/or genotyping the IL4Rα gene in an individual. The methods involve identifying the nucleotide or nucleotide pair present at one or more polymorphic sites selected from PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45 in one or both copies of the IL4Rα gene from the individual. The compositions contain oligonucleotide probes and primers designed to specifically hybridize to one or more target regions containing, or that are adjacent to, a polymorphic site. The methods and compositions for establishing the genotype or haplotype of an individual at the novel polymorphic sites described herein are useful for studying the effect of the polymorphisms in the etiology of diseases affected by the expression and function of the IL4Rα protein, studying the efficacy of drugs targeting IL4Rα, predicting individual susceptibility to diseases affected by the expression and function of the IL4Rα protein and predicting individual responsiveness to drugs targeting IL4Rα.

[0024] In yet another embodiment, the invention provides a method for identifying an association between a genotype or haplotype and a trait. In preferred embodiments, the trait is susceptibility to a disease, severity of a disease, the staging of a disease or response to a drug. Such methods have applicability in developing diagnostic tests and therapeutic treatments for allergies, asthma, and other immune responses.

[0025] The present invention also provides transgenic animals comprising one of the IL4Rα genomic polymorphic variants described herein and methods for producing such animals. The transgenic animals are useful for studying expression of the IL4Rα isogenes in vivo, for in vivo screening and testing of drugs targeted against IL4Rα protein, and for testing the efficacy of therapeutic agents and compounds for allergies, asthma, and other immune responses in a biological system.

[0026] The present invention also provides a computer system for storing and displaying polymorphism data determined for the IL4Rα gene. The computer system comprises a computer processing unit; a display; and a database containing the polymorphism data. The polymorphism data includes the polymorphisms, the genotypes and the haplotypes identified for the IL4Rα gene in a reference population. In a preferred embodiment, the computer system is capable of producing a display showing IL4Rα haplotypes organized according to their evolutionary relationships.

BRIEF DESCRIPTION OF THE DRAWINGS

[0027]FIG. 1 illustrates a reference sequence for the IL4Rα gene that is the reverse complement of part of Genbank Accession Number AC004525.1; contiguous lines; SEQ ID NO:1), with the underlines indicating the start and stop codons, shading indicating the reference coding sequence, and the bold nucleotides indicating the polymorphic sites and polymorphisms identified by Applicants in a reference population.

[0028]FIG. 2 illustrates a reference sequence for the IL4Rα coding sequence (GenBank Accession Number X52425; contiguous lines; SEQ ID NO:2), with the underlines indicating the start and stop codons, and the bold nucleotides indicating the polymorphic sites and polymorphisms identified by Applicants in a reference population.

[0029]FIG. 3 illustrates a reference sequence for the IL4Rα protein (GenBank Accession Number CAA36672; contiguous lines; SEQ ID NO:3), with the bold amino acids indicating the amino acid variations caused by the polymorphisms of FIG. 2.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0030] The present invention is based on the discovery of novel variants of the IL4Rα gene. As described in more detail below, the inventors herein discovered 38 novel polymorphic sites by characterizing the IL4Rα gene found in genomic DNAs isolated from Index Repository IA that contains immortalized cell lines from one chimpanzee and 93 human individuals and Index Repository IB that contains 70 human individuals. Theses two repositories contain 51 individuals in common.

[0031] The human individuals in Index Repository IA included a reference population of 79 unrelated individuals self-identified as belonging to one of four major population groups: Caucasian (22 individuals), African descent (20 individuals) Asian (20 individuals) Hispanic/Latino (17 individuals). To the extent possible, the members of this reference population were organized into population subgroups by the self-identified ethnogeographic origin of their four grandparents as shown in Table 1 below. In addition, Index Repository IA contains three unrelated indigenous American Indians (one from each of North, Central, and South America), one three-generation Caucasian family (From the CEPH Utah cohort) and one two-generation African-American family. TABLE 1 Population Groups in Index Repository IA No. of Population Group Population Subgroup Individuals African descent 20 Sierra Leone 1 Asian 20 Burma 1 China 3 Japan 6 Korea 1 Philippines 5 Vietnam 4 Caucasian 22 British Isles 3 British Isles/Central 4 British Isles/Eastern 1 Central/Eastern 1 Eastern 3 Central/Mediterranean 1 Mediterranean 2 Scandinavian 2 Hispanic/Latino 17 Caribbean 7 Caribbean (Spanish Descent) 2 Central American (Spanish Descent) 1 Mexican American 4 South American (Spanish Descent) 3

[0032] Index Repository IB contains a reference population of 70 human individuals comprised of 4 three-generation families (from the CEPH Utah cohort) as well as unrelated African-American, Asian, and Caucasian individuals. A total of 38 individuals in this reference population are unrelated.

[0033] Using the IL4Rα genotypes identified in the Index Repositories and the methodology described in the Examples below, the inventors herein also determined the haplotypes found on each chromosome for most human members of this repository. The IL4α genotypes and haplotypes found in the Index Repositories include those shown in Tables 4 and 5, respectively. The polymorphism and haplotype data disclosed herein are useful for studying population diversity, anthropological lineage, the significance of diversity and lineage at the phenotypic level, paternity testing, forensic applications, and for identifying associations between the IL4Rα genetic variation and a trait such as level of drug response or susceptibility to disease.

[0034] In the context of this disclosure, the following terms shall be defined as follows unless otherwise indicated:

[0035] Allele—A particular form of a genetic locus, distinguished from other forms by its particular nucleotide sequence.

[0036] Candidate Gene—A gene which is hypothesized to be responsible for a disease, condition, or the response to a treatment, or to be correlated with one of these.

[0037] Gene—A segment of DNA that contains all the information for the regulated biosynthesis of an RNA product, including promoters, exons, introns, and other untranslated regions that control expression.

[0038] Genotype—An unphased 5′ to 3′ sequence of nucleotide pair(s) found at one or more polymorphic sites in a locus on a pair of homologous chromosomes in an individual. As used herein, genotype includes a full-genotype and/or a sub-genotype as described below.

[0039] Full-genotype—The unphased 5′ to 3′ sequence of nucleotide pairs found at all known polymorphic sites in a locus on a pair of homologous chromosomes in a single individual.

[0040] Sub-genotype—The unphased 5′ to 3′ sequence of nucleotides seen at a subset of the known polymorphic sites in a locus on a pair of homologous chromosomes in a single individual.

[0041] Genotyping—A process for determining a genotype of an individual.

[0042] Haplotype—A 5′ to 3′ sequence of nucleotides found at one or more polymorphic sites in a locus on a single chromosome from a single individual. As used herein, haplotype includes a fall-haplotype and/or a sub-haplotype as described below.

[0043] Full-haplotype—The 5′ to 3′ sequence of nucleotides found at all known polymorphic sites in a locus on a single chromosome from a single individual.

[0044] Sub-haplotype—The 5′ to 3′ sequence of nucleotides seen at a subset of the known polymorphic sites in a locus on a single chromosome from a single individual.

[0045] Haplotype pair—The two haplotypes found for a locus in a single individual.

[0046] Haplotyping—A process for determining one or more haplotypes in an individual and includes use of family pedigrees, molecular techniques and/or statistical inference.

[0047] Haplotype data—Information concerning one or more of the following for a specific gene: a listing of the haplotype pairs in each individual in a population; a listing of the different haplotypes in a population; frequency of each haplotype in that or other populations, and any known associations between one or more haplotypes and a trait.

[0048] Isoform—A particular form of a gene, mRNA, cDNA or the protein encoded thereby, distinguished from other forms by its particular sequence and/or structure.

[0049] Isogene—One of the isoforms of a gene found in a population. An isogene contains all of the polymorphisms present in the particular isoform of the gene.

[0050] Isolated—As applied to a biological molecule such as RNA, DNA, oligonucleotide, or protein, isolated means the molecule is substantially free of other biological molecules such as nucleic acids, proteins, lipids, carbohydrates, or other material such as cellular debris and growth media. Generally, the term “isolated” is not intended to refer to a complete absence of such material or to absence of water, buffers, or salts, unless they are present in amounts that substantially interfere with the methods of the present invention.

[0051] Locus—A location on a chromosome or DNA molecule corresponding to a gene or a physical or phenotypic feature.

[0052] Naturally-occurring—A term used to designate that the object it is applied to, e.g., naturally-occurring polynucleotide or polypeptide, can be isolated from a source in nature and which has not been intentionally modified by man.

[0053] Nucleotide pair—The nucleotides found at a polymorphic site on the two copies of a chromosome from an individual.

[0054] Phased—As applied to a sequence of nucleotide pairs for two or more polymorphic sites in a locus, phased means the combination of nucleotides present at those polymorphic sites on a single copy of the locus is known.

[0055] Polymorphic site (PS)—A position within a locus at which at least two alternative sequences are found in a population, the most frequent of which has a frequency of no more than 99%.

[0056] Polymorphic variant—A gene, mRNA, cDNA, polypeptide or peptide whose nucleotide or amino acid sequence varies from a reference sequence due to the presence of a polymorphism in the gene.

[0057] Polymorphism—The sequence variation observed in an individual at a polymorphic site. Polymorphisms include nucleotide substitutions, insertions, deletions and microsatellites and may, but need not, result in detectable differences in gene expression or protein function.

[0058] Polymorphism data—Information concerning one or more of the following for a specific gene: location of polymorphic sites; sequence variation at those sites; frequency of polymorphisms in one or more populations; the different genotypes and/or haplotypes determined for the gene; frequency of one or more of these genotypes and/or haplotypes in one or more populations; any known association(s) between a trait and a genotype or a haplotype for the gene.

[0059] Polymorphism Database—A collection of polymorphism data arranged in a systematic or methodical way and capable of being individually accessed by electronic or other means.

[0060] Polynucleotide—A nucleic acid molecule comprised of single-stranded RNA or DNA or comprised of complementary, double-stranded DNA.

[0061] Population Group—A group of individuals sharing a common ethnogeographic origin.

[0062] Reference Population—A group of subjects or individuals who are predicted to be representative of the genetic variation found in the general population. Typically, the reference population represents the genetic variation in the population at a certainty level of at least 85%, preferably at least 90%, more preferably at least 95% and even more preferably at least 99%.

[0063] Single Nucleotide Polymorphism (SNP)—Typically, the specific pair of nucleotides observed at a single polymorphic site. In rare cases, three or four nucleotides may be found.

[0064] Subject—A human individual whose genotypes or haplotypes or response to treatment or disease state are to be determined.

[0065] Treatment—A stimulus administered internally or externally to a subject.

[0066] Unphased—As applied to a sequence of nucleotide pairs for two or more polymorphic sites in a locus, unphased means the combination of nucleotides present at those polymorphic sites on a single copy of the locus is not known.

[0067] The inventors herein have discovered 38 novel polymorphic sites, and confirmed the existence of 7 other sites, in the IL4Rα gene. The polymorphic sites identified by the inventors are referred to as PS1-45 to designate the order in which they are located in the gene (see Table 3 below), with the novel polymorphic site referred to as PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45 and the previously reported poly sites referred to as PS5, PS24, PS26, PS29, PS31, PS42, and PS43.

[0068] Thus, in one embodiment, the invention provides an isolated polynucleotide comprising a polymorphic variant of the IL4Rα gene or a fragment of the gene which contains at least one of the novel polymorphic sites described herein. The nucleotide sequence of a variant IL4Rα gene is identical to the reference genomic sequence for those portions of the gene examined, as described in the Examples below, except that it comprises a different nucleotide at one or more of the novel polymorphic sites PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45, and may also comprise one or more additional polymorphisms selected from the group consisting of PS5, PS24, PS26, PS29, PS31, PS42, and PS43. Similarly, the nucleotide sequence of a variant fragment of the IL4Rα gene is identical to the corresponding portion of the reference sequence except for having a different nucleotide at one or more of the novel polymorphic sites described herein. Thus, the invention specifically does not include polynucleotides comprising a nucleotide sequence identical to the reference sequence (or other reported IL4Rα sequences) or to portions of the reference sequence (or other reported IL4Rα sequences), except for genotyping oligonucleotides as described below.

[0069] The location of a polymorphism in a variant gene or fragment is identified by aligning its sequence against SEQ ED NO:1. The polymorphism is selected from the group consisting of guanine at PS1, thymine at PS2, thymine at PS3, cytosine at PS4, thymine at PS6, adenine at PS7, cytosine at PS8, thymine at PS9, thymine at PS10, adenine at PS11, adenine at PS12, thymine at PS13, thymine at PS14, adenine at PS15, thymine at PS16, adenine at PS17, thymine at PS18, adenine at PS19, cytosine at PS20, cytosine at PS21, thymine at PS22, cytosine at PS23, thymine at PS25, thymine at PS27, cytosine at PS28, thymine at PS30, adenine at PS32, thymine at PS33, guanine at PS34, cytosine at PS35, cytosine at PS36, cytosine at PS37, thymine at PS38, guanine at PS39, guanine at PS40, adenine at PS41, thymine at PS44, and adenine at PS45. In a preferred embodiment, the polymorphic variant comprises a naturally-occurring isogene of the IL4Rα gene which is defined by any one of haplotypes 1-53 shown in Table 5 below.

[0070] Polymorphic variants of the invention may be prepared by isolating a clone containing the IL4Rα gene from a human genomic library. The clone may be sequenced to determine the identity of the nucleotides at the polymorphic sites described herein. Any particular variant claimed herein could be prepared from this clone by performing in vitro mutagenesis using procedures well-known in the art.

[0071] IL4Rα isogenes may be isolated using any method that allows separation of the two “copies” of the IL4Rα gene present in an individual, which, as readily understood by the skilled artisan, may be the same allele or different alleles. Separation methods include targeted in vivo cloning (TIVC) in yeast as described in WO 98/01573, U.S. Pat. No. 5,866,404, and copending U.S. application Serial No. 08/987,966. Another method, which is described in copending U.S. application Ser. No. 08/987,966, uses an allele specific oligonucleotide in combination with primer extension and exonuclease degradation to generate hemizygous DNA targets. Yet other methods are single molecule dilution (SMD) as described in Ruaño et al., Proc. Natl. Acad. Sci. 87:6296-6300, 1990; and allele specific PCR (Ruaño et al., 17 Nucleic Acids. Res. 8392, 1989; Ruaño et al., 19 Nucleic Acids Res. 6877-6882, 1991; Michalatos-Beloin et al., 24 Nucleic Acids Res. 4841-4843, 1996).

[0072] The invention also provides IL4Rα genome anthologies, which are collections of IL4Rα isogenes found in a given population. The population may be any group of at least two individuals, including but not limited to a reference population, a population group, a family population, a clinical population, and a same sex population. An IL4Rα genome anthology may comprise individual IL4Rα isogenes stored in separate containers such as microtest tubes, separate wells of a microtitre plate and the like. Alternatively, two or more groups of the IL4Rα isogenes in the anthology may be stored in separate containers. Individual isogenes or groups of isogenes in a genome anthology may be stored in any convenient and stable form, including but not limited to in buffered solutions, as DNA precipitates, freeze-dried preparations and the like. A preferred IL4Rα genome anthology of the invention comprises a set of isogenes defined by the haplotypes shown in Table 5 below.

[0073] An isolated polynucleotide containing a polymorphic variant nucleotide sequence of the invention may be operably linked to one or more expression regulatory elements in a recombinant expression vector capable of being propagated and expressing the encoded IL4Rα protein in a prokaryotic or a eukaryotic host cell. Examples of expression regulatory elements which may be used include, but are not limited to, the lac system, operator and promoter regions of phage lambda, yeast promoters, and promoters derived from vaccinia virus, adenovirus, retroviruses, or SV40. Other regulatory elements include, but are not limited to, appropriate leader sequences, termination codons, polyadenylation signals, and other sequences required for the appropriate transcription and subsequent translation of the nucleic acid sequence in a given host cell. Of course, the correct combinations of expression regulatory elements will depend on the host system used. In addition, it is understood that the expression vector contains any additional elements necessary for its transfer to and subsequent replication in the host cell. Examples of such elements include, but are not limited to, origins of replication and selectable markers. Such expression vectors are commercially available or are readily constructed using methods known to those in the art (e.g., F. Ausubel et al., 1987, in “Current Protocols in Molecular Biology”, John Wiley and Sons, New York, N.Y.). Host cells which may be used to express the variant IL4Rα sequences of the invention include, but are not limited to, eukaryotic and mammalian cells, such as animal, plant, insect and yeast cells, and prokaryotic cells, such as E. coli, or algal cells as known in the art. The recombinant expression vector may be introduced into the host cell using any method known to those in the art including, but not limited to, microinjection, electroporation, particle bombardment, transduction, and transfection using DEAE-dextran, lipofection, or calcium phosphate (see e.g., Sambrook et al. (1989) in “Molecular Cloning. A Laboratory Manual”, Cold Spring Harbor Press, Plainview, N.Y.). In a preferred aspect, eukaryotic expression vectors that function in eukaryotic cells, and preferably mammalian cells, are used. Non-limiting examples of such vectors include vaccinia virus vectors, adenovirus vectors, herpes virus vectors, and baculovirus transfer vectors. Preferred eukaryotic cell lines include COS cells, CHO cells, HeLa cells, NIH/3T3 cells, and embryonic stem cells (Thomson, J. A. et al., 1998 Science 282:1145-1147). Particularly preferred host cells are mammalian cells.

[0074] As will be readily recognized by the skilled artisan, expression of polymorphic variants of the IL4Rα gene will produce IL4Rα mRNAs varying from each other at any polymorphic site retained in the spliced and processed mRNA molecules. These mRNAs can be used for the preparation of an IL4Rα cDNA comprising a nucleotide sequence which is a polymorphic variant of the IL4Rα reference coding sequence shown in FIG. 2. Thus, the invention also provides IL4Rα mRNAs and corresponding cDNAs which comprise a nucleotide sequence that is identical to SEQ ID NO:2 (FIG. 2), or its corresponding RNA sequence, except for having one or more polymorphisms selected from the group consisting of thymine at a position corresponding to nucleotide 237, adenine at a position corresponding to nucleotide 244, cytosine at a position corresponding to nucleotide 291, thymine at a position corresponding to nucleotide 501, adenine at a position corresponding to nucleotide 554, cytosine at a position corresponding to nucleotide 939, thymine at a position corresponding to nucleotide 1242, thymine at a position corresponding to nucleotide 1293, cytosine at a position corresponding to nucleotide 1299, thymine at a position corresponding to nucleotide 1701, adenine at a position corresponding to nucleotide 1735, thymine at a position corresponding to nucleotide 2023, guanine at a position corresponding to nucleotide 2254 and cytosine at a position corresponding to nucleotide 2397, and may also comprise one or more additional polymorphisms selected from the group consisting of guanine at a position corresponding to 223, cytosine at a position corresponding to nucleotide 1199, cytosine at a position corresponding to 1291, cytosine at a position corresponding to nucleotide 1507 and guanine at a position corresponding to 1737. Fragments of these variant mRNAs and cDNAs are included in the scope of the invention, provided they contain the novel polymorphisms described herein. The invention specifically excludes polynucleotides identical to previously identified and characterized IL4Rα cDNAs and fragments thereof. Polynucleotides comprising a variant RNA or DNA sequence may be isolated from a biological sample using well-known molecular biological procedures or may be chemically synthesized.

[0075] Genomic and cDNA fragments of the invention comprise at least one novel polymorphic site identified herein and have a length of at least 10 nucleotides and may range up to the full length of the gene. Preferably, a fragment according to the present invention is between 100 and 3000 nucleotides in length, and more preferably between 200 and 2000 nucleotides in length, and most preferably between 500 and 1000 nucleotides in length.

[0076] In describing the polymorphic sites identified herein, reference is made to the sense strand of the gene for convenience. However, as recognized by the skilled artisan, nucleic acid molecules containing the IL4Rα gene may be complementary double stranded molecules and thus reference to a particular site on the sense strand refers as well to the corresponding site on the complementary antisense strand. Thus, reference may be made to the same polymorphic site on either strand and an oligonucleotide may be designed to hybridize specifically to either strand at a target region containing the polymorphic site. Thus, the invention also includes single-stranded polynucleotides which are complementary to the sense strand of the IL4Rα genomic variants described herein.

[0077] Polynucleotides comprising a polymorphic gene variant or fragment may be useful for therapeutic purposes. For example, where a patient could benefit from expression, or increased expression, of a particular IL4Rα protein isoform, an expression vector encoding the isoform may be administered to the patient. The patient may be one who lacks the IL4Rα isogene encoding that isoform or may already have at least one copy of that isogene.

[0078] In other situations, it may be desirable to decrease or block expression of a particular IL4Rα isogene. Expression of an IL4Rα isogene may be turned off by transforming a targeted organ, tissue or cell population with an expression vector that expresses high levels of untranslatable mRNA for the isogene. Alternatively, oligonucleotides directed against the regulatory regions (e.g., promoter, introns, enhancers, 3′ untranslated region) of the isogene may block transcription. Oligonucleotides targeting the transcription initiation site, e.g., between positions −10 and +10 from the start site are preferred. Similarly, inhibition of transcription can be achieved using oligonucleotides that base-pair with region(s) of the isogene DNA to form triplex DNA (see e.g., Gee et al. in Huber, B. E. and B. I. Carr, Molecular and Immunologic Approaches, Futura Publishing Co., Mt. Kisco, N.Y., 1994). Antisense oligonucleotides may also be designed to block translation of IL4Rα mRNA transcribed from a particular isogene. It is also contemplated that ribozymes may be designed that can catalyze the specific cleavage of IL4Rα mRNA transcribed from a particular isogene.

[0079] The oligonucleotides may be delivered to a target cell or tissue by expression from a vector introduced into the cell or tissue in vivo or ex vivo. Alternatively, the oligonucleotides may be formulated as a pharmaceutical composition for administration to the patient. Oligoribonucleotides and/or oligodeoxynucleotides intended for use as antisense oligonucleotides may be modified to increase stability and half-life. Possible modifications include, but are not limited to phosphorothioate or 2′ O-methyl linkages, and the inclusion of nontraditional bases such as inosine and queosine, as well as acetyl-, methyl-, thio-, and similarly modified forms of adenine, cytosine, guanine, thymine, and uracil which are not as easily recognized by endogenous nucleases.

[0080] The invention also provides an isolated polypeptide comprising a polymorphic variant of the reference IL4Rα amino acid sequence shown in 3. The location of a variant amino acid in an IL4Rα polypeptide or fragment of the invention is identified by aligning its sequence against FIG. 3. An IL4Rα protein variant of the invention comprises an amino acid sequence identical to SEQ ID NO: 3 except for having one or more variant amino acids selected from the group consisting of threonine at a position corresponding to amino acid 82, histidine at a position corresponding to amino acid 185, isoleucine at a position corresponding to amino acid 579, serine at a position corresponding to amino acid 675, and alanine at a position corresponding to amino acid 752, and may also comprise one or more additional variant amino acids selected from the group consisting of valine at a position corresponding to amino acid 75, alanine at a position corresponding to amino acid 400, arginine at a position correpsonding to amino acid 431, proline at a position corresponding to amino acid 503, and arginine at a position corresponding to amino acid 576. The invention specifically excludes amino acid sequences identical to those previously identified for IL4Rα including SEQ ID NO: 3, and previously described fragments thereof. IL4Rα protein variants included within the invention comprise all amino acid sequences based on SEQ ID NO: 3 and having the combination of amino acid variations described in Table 2 below. In preferred embodiments, an IL4Rα protein variant of the invention is encoded by an isogene defined by one of the observed haplotypes shown in Table 5. TABLE 2 Novel Polymorphic Variant of IL4R^(α) Polymorphic Variant Amino Acid Position and Identities Number 75 82 185 400 431 503 576 579 675 752 1 I A R E C S Q V P A 2 I A R E C S Q V S S 3 I A R E C S Q V S A 4 I A R E C S Q I P S 5 I A R E C S Q I P A 6 I A R E C S Q I S S 7 I A R E C S Q I S A 8 I A R E C S R V P A 9 I A R E C S R V S S 10 I A R E C S R V S A 11 I A R E C S R I P S 12 I A R E C S R I P A 13 I A R E C S R I S S 14 I A R E C S R I S A 15 I A R E C P Q V P A 16 I A R E C P Q V S S 17 I A R E C P Q V S A 18 I A R E C P Q I P S 19 I A R E C P Q I P A 20 I A R E C P Q I S S 21 I A R E C P Q I S A 22 I A R E C P R V P A 23 I A R E C P R V S S 24 I A R E C P R V S A 25 I A R E C P R I P S 26 I A R E C P R I P A 27 I A R E C P R I S S 28 I A R E C P R I S A 29 I A R E R S Q V P A 30 I A R E R S Q V S S 31 I A R E R S Q V S A 32 I A R E R S Q I P S 33 I A R E R S Q I P A 34 I A R E R S Q I S S 35 I A R E R S Q I S A 36 I A R E R S R V P A 37 I A R E R S R V S S 38 I A R E R S R V S A 39 I A R E R S R I P S 40 I A R E R S R I P A 41 I A R E R S R I S S 42 I A R E R S R I S A 43 I A R E R P Q V P A 44 I A R E R P Q V S S 45 I A R E R P Q V S A 46 I A R E R P Q I P S 47 I A R E R P Q I P A 48 I A R E R P Q I S S 49 I A R E R P Q I S A 50 I A R E R P R V P A 51 I A R E R P R V S S 52 I A R E R P R V S A 53 1 A R E R P R I P S 54 I A R E R P R I P A 55 I A R E R P R I S S 56 I A R E R P R I S A 57 I A R A C S Q V P A 58 I A R A C S Q V S S 59 I A R A C S Q V S A 60 I A R A C S Q I P S 61 I A R A C S Q I P A 62 I A R A C S Q I S S 63 I A R A C S Q I S A 64 I A R A C S R V P A 65 I A R A C S R V S S 66 I A R A C S R V S A 67 I A R A C S R I P S 68 I A R A C S R I P A 69 I A R A C S R I S S 70 I A R A C S R I S A 71 I A R A C P Q V P A 72 I A R A C P Q V S S 73 I A R A C P Q V S A 74 I A R A C P Q I P S 75 I A R A C P Q I P A 76 I A R A C P Q I S S 77 I A R A C P Q I S A 78 I A R A C P R V P A 79 I A R A C P R V S S 80 I A R A C P R V S A 81 I A R A C P R I P S 82 I A R A C P R I P A 83 I A R A C P R I S S 84 I A R A C P R I S A 85 I A R A R S Q V P A 86 I A R A R S Q V S S 87 I A R A R S Q V S A 88 I A R A R S Q I P S 89 I A R A R S Q I P A 90 I A R A R S Q I S S 91 I A R A R S Q I S A 92 I A R A R S R V P A 93 I A R A R S R V S S 94 i A R A R S R V S A 95 i A R A R S R I P S 96 I A R A R S R I P A 97 I A R A R S R I S S 98 I A R A R S R I S A 99 I A R A R P Q V P A 100 I A R A R P Q V S S 101 I A R A R P Q V S A 102 I A R A R P Q I P S 103 I A R A R P Q I P A 104 I A R A R P Q I S S 105 I A R A R P Q I S A 106 I A R A R P R V P A 107 I A R A R P R V S S 108 I A R A R P R V S A 109 I A R A R P R I P S 110 I A R A R P R I P A 111 I A R A R P R I S S 112 i A R A R P R I S A 113 I A H E C S Q V P S 114 I A H E C S Q V P A 115 I A H E C S Q V S S 116 I A H E C S Q V S A 117 I A H E C S Q I P S 118 I A H E C S Q I P A 119 I A H E C S Q I S S 120 I A H E C S Q I S A 121 I A H E C S R V P S 122 I A H E C S R V P A 123 I A H E C S R V S S 124 I A H E C S R V S A 125 I A H E C S R I P S 126 I A H E C S R I P A 127 I A H E C S R I S S 128 I A H E C S R I S A 129 I A H E C P Q V P S 130 I A H E C P Q V P A 131 I A H E C P Q V S S 132 I A H E C P Q V S A 133 I A H E C P Q I P S 134 I A H E C P Q I P A 135 I A H E C P Q I S S 136 I A H E C P Q I S A 137 I A H E C P R V P S 138 I A H E C P R V P A 139 I A H E C P R V S S 140 I A H E C P R V S A 141 I A H E C P R I P S 142 I A H E C P R I P A 143 I A H E C P R I S S 144 I A H E C P R I S A 145 I A H E R S Q V P S 146 I A H E R S Q V P A 147 I A H E R S Q V S S 148 I A H E R S Q V S A 149 I A H E R S Q I P S 150 I A H E R S Q I P A 151 I A H E R S Q I S S 152 I A H E R S Q I S A 153 I A H E R S R V P S 154 I A H E R S R V P A 155 I A H E R S R V S S 156 I A H E R S R V S A 157 I A H E R S R I P S 158 I A H E R S R I P A 159 I A H E R S R I S S 160 I A H E R S R I S A 161 I A H E R P Q V P S 162 I A H E R P Q V P A 163 I A H E R P Q V S S 164 I A H E R P Q V S A 165 I A H E R P Q I P S 166 I A H E R P Q I P A 167 I A H E R P Q I S S 168 I A H E R P Q I S A 169 I A H E R P R V P S 170 I A H E R P R V P A 171 I A H E R P R V S S 172 I A H E R P R V S A 173 I A H E R P R I P S 174 I A H E R P R I P A 175 I A H E R P R I S S 176 I A H E R P R I S A 177 I A H A C S Q V P S 178 I A H A C S Q V P A 179 I A H A C S Q V S S 180 I A H A C S Q V S A 181 I A H A C S Q I P S 182 I A H A C S Q I P A 183 I A H A C S Q I S S 184 I A H A C S Q I S A 185 I A H A C S R V P S 186 I A H A C S R V P A 187 I A H A C S R V S S 188 I A H A C S R V S A 189 I A H A C S R I P S 190 I A H A C S R I P A 191 i A H A C S R I S S 192 I A H A C S R I S A 193 I A H A C P Q V P S 194 I A H A C P Q V P A 195 I A H A C P Q V S S 196 I A H A C P Q V S A 197 I A H A C P Q I P S 198 I A H A C P Q I P A 199 I A H A C P Q I S S 200 I A H A C P Q I S A 201 I A H A C P R V P S 202 I A H A C P R V P A 203 I A H A C P R V S S 204 I A H A C P R V S A 205 I A H A C P R I P S 206 I A H A C P R I P A 207 I A H A C P R I S S 208 I A H A C P R I S A 209 I A H A R S Q V P S 210 I A H A R S Q V P A 211 I A H A R S Q V S S 212 I A H A R S Q V S A 213 I A H A R S Q I P S 214 I A H A R S Q I P A 215 I A H A R S Q I S S 216 I A H A R S Q I S A 217 I A H A R S R V P S 218 I A H A R S R V P A 219 I A H A R S R V S S 220 I A H A R S R V S A 221 I A H A R S R I P S 222 I A H A R S R I P A 223 I A H A R S R I S S 224 I A H A R S R I S A 225 I A H A R P Q V P S 226 I A H A R P Q V P A 227 I A H A R P Q V S S 228 I A H A R P Q V S A 229 I A H A R P Q I P S 230 1 A H A R P Q I P A 231 I A H A R P Q I S S 232 I A H A R P Q I S A 233 I A H A R P R V P S 234 I A H A R P R V P A 235 I A H A R P R V S S 236 I A H A R P R V S A 237 I A H A R P R I P S 238 I A H A R P R I P A 239 I A H A R P R I S S 240 I A H A R P R I S A 241 I T R E C S Q V P S 242 I T R E C S Q V P A 243 I T R E C S Q V S S 244 I T R E C S Q V S A 245 I T R E C S Q I P S 246 I T R E C S Q I P A 247 I T R E C S Q I S S 248 I T R E C S Q I S A 249 1 T R E C S R V P S 250 I T R E C S R V P A 251 I T R E C S R V S S 252 I T R E C S R V S A 253 I T R E C S R I P S 254 I T R E C S R I P A 255 I T R E C S R I S S 256 I T R E C S R I S A 257 I T R E C P Q V P S 258 I T R E C P Q V P A 259 I T R E C P Q V S S 260 I T R E C P Q V S A 261 I T R E C P Q I P S 262 I T R E C P Q I P A 263 I T R E C P Q I S S 264 I T R E C P Q I S A 265 I T R E C P R V P S 266 I T R E C P R V P A 267 I T R E C P R V S S 268 I T R E C P R V S A 269 I T R E C P R I P S 270 I T R E C P R I P A 271 I T R E C P R I S S 272 I T R E C P R I S A 273 I T R E R S Q V P S 274 I T R E R S Q V P A 275 I T R E R S Q V S S 276 I T R E R S Q V S A 277 I T R E R S Q I P S 278 I T R E R S Q I P A 279 I T R E R S Q I S S 280 1 T R E R S Q I S A 281 I T R E R S R V P S 282 I T R E R S R V P A 283 I T R E R S R V S S 284 I T R F R S R V S A 285 I T R F R S R I P S 286 I T R E R S R I P A 287 I T R E R S R I S S 288 I T R E R S R I S A 289 I T R F R P Q V P S 290 I T R E R P Q V P A 291 I T R F R P Q V S S 292 I T R E R P Q V S A 293 I T R F R P Q I P S 294 I T R E R P Q I P A 295 I T R F R P Q I S S 296 I T R E R P Q I S A 297 I T R E R P R V P S 298 I T R E R P R V P A 299 I T R E R P R V S S 300 I T R F R P R V S A 301 I T R F R P R I P S 302 I T R E R P R I P A 303 I T R E R P R I S S 304 I T R E R P R I S A 305 I T R A C S Q V P S 315 I T R A C S R V S S 316 I T R A C S R V S A 317 I T R A C S R I P S 318 I T R A C S R I P A 319 I T R A C S R I S S 320 I T R A C S R I S A 321 I T R A C P Q V P S 322 I T R A C P Q V P A 323 I T R A C P Q V S S 324 I T R A C P Q V S A 325 I T R A C P Q I P S 326 I T R A C P Q I P A 327 I T R A C P Q I S S 328 I T R A C P Q I S A 306 I T R A C S Q V P A 307 I T R A C S Q V S S 308 I T R A C S Q V S A 309 I T R A C S Q I P S 310 I T R A C S Q I P A 311 I T R A C S Q I S S 312 I T R A C S Q I S A 313 I T R A C S R V P S 314 I T R A C S R V P A 329 I T R A C P R V P S 330 I T R A C P R V P A 331 I T R A C P R V S S 332 I T R A C P R V S A 333 I T R A C P R I P S 334 I T R A C P R I P A 335 I T R A C P R I S S 336 I T R A C P R I S A 337 I T R A R S Q V P S 338 I T R A R S Q V P A 339 I T R A R S Q V S S 340 I T R A R S Q V S A 341 I T R A R S Q I P S 342 I T R A R S Q I P A 343 I T R A R S Q I S S 344 I T R A R S Q I S A 345 I T R A R S R V P S 346 I T R A R S R V P A 347 I T R A R S R V S S 348 I T R A R S R V S A 349 I T R A R S R I P S 350 I T R A R S R I P A 351 I T R A R S R I S S 352 I T R A R S R I S A 353 I T R A R P Q V P S 354 I T R A R P Q V P A 355 I T R A R P Q V S S 356 I T R A R P Q V S A 357 I T R A R P Q I P S 358 I T R A R P Q I P A 359 I T R A R P Q I S S 360 I T R A R P Q I S A 361 I T R A R P R V P S 362 I T R A R P R V P A 363 I T R A R P R V S S 364 I T R A R P R V S A 365 I T R A R P R I P S 366 I T R A R P R I P A 367 I T R A R P R I S S 368 I T R A R P R I S A 369 I T H E C S Q V P S 370 I T H E C S Q V P A 371 I T H E C S Q V S S 372 I T H E C S Q V S A 373 I T H E C S Q I P S 374 I T H E C S Q I P A 375 I T H E C S Q I S S 376 I T H E C S Q I S A 377 I T H E C S R V P S 378 I T H E C S R V P A 379 I T H E C S R V S S 380 I T H E C S R V S A 381 I T H E C S R I P S 382 I T H E C S R I P A 383 I T H E C S R I S S 384 I T H E C S R I S A 385 I T H E C P Q V P S 386 I T H E C P Q V P A 387 I T H E C P Q V S S 388 I T H E C P Q V S A 389 I T H E C P Q I P S 390 I T H E C P Q I P A 391 I T H E C P Q I S S 392 I T H E C P Q I S A 393 I T H E C P R V P S 394 I T H E C P R V P A 395 I T H E C P R V S S 396 I T H E C P R V S A 397 I T H E C P R I P S 398 I T H E C P R I P A 399 I T H E C P R I S S 400 I T H E C P R I S A 401 I T H E R S Q V P S 402 I T H E R S Q V P A 403 I T H E R S Q V S S 404 I T H E R S Q V S A 405 I T H E R S Q I P S 406 I T H E R S Q I P A 407 I T H E R S Q I S S 408 I T H E R S Q I S A 409 I T H E R S R V P S 410 I T H E R S R V P A 411 I T H E R S R V S S 412 I T H E R S R V S A 413 I T H E R S R I P S 414 I T H E R S R I P A 415 I T H E R S R I S S 416 I T H E R S R I S A 417 I T H E R P Q V P S 418 I T H E R P Q V P A 419 I T H E R P Q V S S 420 I T H E R P Q V S A 421 I T H E R P Q I P S 422 I T H E R P Q I P A 423 I T H E R P Q I S S 424 I T H E R P Q I S A 425 I T H E R P R V P S 426 I T H E R P R V P A 427 I T H E R P R V S S 428 I T H E R P R V S A 429 I T H E R P R I P S 430 I T H E R P R I P A 431 I T H E R P R I S S 432 I T H E R P R I S A 433 I T H A C S Q V P S 434 I T H A C S Q V P A 435 I T H A C S Q V S S 436 I T H A C S Q V S A 437 I T H A C S Q I P S 438 I T H A C S Q I P A 439 I T H A C S Q I S S 440 I T H A C S Q I S A 441 I T H A C S R V P S 442 I T H A C S R V P A 443 I T H A C S R V S S 444 I T H A C S R V S A 445 I T H A C S R I P S 446 I T H A C S R I P A 447 I T H A C S R I S S 448 I T H A C S R I S A 449 I T H A C P Q V P S 450 I T H A C P Q V P A 451 I T H A C P Q V S S 452 I T H A C P Q V S A 453 I T H A C P Q I P S 454 I T H A C P Q I P A 455 I T H A C P Q I S S 456 I T H A C P Q I S A 457 I T H A C P R V P S 458 I T H A C P R V P A 459 I T H A C P R V S S 460 I T H A C P R V S A 461 I T H A C P R I P S 462 I T H A C P R I P A 463 I T H A C P R I S S 464 I T H A C P R I S A 465 I T H A R S Q V P S 466 I T H A R S Q V P A 467 I T H A R S Q V S S 468 I T H A R S Q V S A 469 I T H A R S Q I P S 470 I T H A R S Q I P A 471 I T H A R S Q I S S 472 I T H A R S Q I S A 473 I T H A R S R V P S 474 I T H A R S R V P A 475 I T H A R S R V S S 476 I T H A R S R V S A 477 I T H A R S R I P S 478 I T H A R S R I P A 479 I T H A R S R I S S 480 I T H A R S R I S A 481 I T H A R P Q V P S 482 I T H A R P Q V P A 483 I T H A R P Q V S S 484 I T H A R P Q V S A 485 I T H A R P Q I P S 486 I T H A R P Q I P A 487 I T H A R P Q I S S 488 I T H A R P Q I S A 489 I T H A R P R V P S 490 I T H A R P R V P A 491 I T H A R P R V S S 492 I T H A R P R V S A 493 I T H A R P R I P S 494 I T H A R P R I P A 495 I T H A R P R I S S 496 I T H A R P R I S A 497 V A R E C S Q V P A 498 V A R F C S Q V S S 499 V A R E C S Q V S A 500 V A R F C S Q I P S 501 V A R F C S Q I P A 502 V A R E C S Q I S S 503 V A R E C S Q I S A 504 V A R E C S R V P A 505 V A R E C S R V S S 506 V A R E C S R V S A 507 V A R E C S R I P S 508 V A R E C S R I P A 509 V A R E C S R I S S 510 V A R E C S R I S A 511 V A R E C P Q V P A 512 V A R E C P Q V S S 513 V A R E C P Q V S A 514 V A R F C P Q I P S 515 V A R F C P Q I P A 516 V A R E C P Q I S S 517 V A R E C P Q I S A 518 V A R E C P R V P A 519 V A R E C P R V S S 520 V A R E C P R V S A 521 V A R E C P R I P S 522 V A R E C P R I P A 523 V A R E C P R I S S 524 V A R E C P R I S A 525 V A R E R S Q V P A 526 V A R E R S Q V S S 527 V A R E R S Q V S A 528 V A R F R S Q I P S 529 V A R F R S Q I P A 530 V A R F R S Q I S S 531 V A R E R S Q I S A 532 V A R E R S R V P A 533 V A R E R S R V S S 534 V A R E R S R V S A 535 V A R E R S R I P S 536 V A R E R S R I P A 537 V A R E R S R I S S 538 V A R E R S R I S A 539 V A R E R P Q V P A 540 V A R E R P Q V S S 541 V A R E R P Q V S A 542 V A R E R P Q I P S 543 V A R E R P Q I P A 544 V A R E R P Q I S S 545 V A R E R P Q I S A 546 V A R E R P R V P A 547 V A R E R P R V S S 548 V A R E R P R V S A 549 V A R E R P R I P S 550 V A R E R P R I P A 551 V A R E R P R I S S 552 V A R E R P R I S A 553 V A R A C S Q V P A 554 V A R A C S Q V S S 555 V A R A C S Q V S A 556 V A R A C S Q I P S 557 V A R A C S Q I P A 558 V A R A C S Q I S S 559 V A R A C S Q I S A 560 V A R A C S R V P A 561 V A R A C S R V S S 562 V A R A C S R V S A 563 V A R A C S R I P S 564 V A R A C S R I P A 565 V A R A C S R I S S 566 V A R A C S R I S A 567 V A R A C P Q V P A 568 V A R A C P Q V S S 569 V A R A C P Q V S A 570 V A R A C P Q I P S 571 V A R A C P Q I P A 572 V A R A C P Q I S S 573 V A R A C P Q I S A 574 V A R A C P R V P A 575 V A R A C P R V S S 576 V A R A C P R V S A 577 V A R A C P R I P S 578 V A R A C P R I P A 579 V A R A C P R I S S 580 V A R A C P R I S A 581 V A R A R S Q V P A 582 V A R A R S Q V S S 583 V A R A R S Q V S A 584 V A R A R S Q I P S 585 V A R A R S Q I P A 586 V A R A R S Q I S S 587 V A R A R S Q I S A 588 V A R A R S R V P A 589 V A R A R S R V S S 590 V A R A R S R V S A 591 V A R A R S R I P S 592 V A R A R S R I P A 593 V A R A R S R I S S 594 V A R A R S R I S A 595 V A R A R P Q V P A 596 V A R A R P Q V S S 597 V A R A R P Q V S A 598 V A R A R P Q I P S 599 V A R A R P Q I P A 600 V A R A R P Q I S S 601 V A R A R P Q I S A 602 V A R A R P R V P A 603 V A R A R P R V S S 604 V A R A R P R V S A 605 V A R A R P R I P S 606 V A R A R P R I P A 607 V A R A R P R I S S 608 V A R A R P R I S A 609 V A H E C S Q V P S 610 V A H E C S Q V P A 611 V A H E C S Q V S S 612 V A H E C S Q V S A 613 V A H E C S Q I P S 614 V A H E C S Q I P A 615 V A H E C S Q I S S 616 V A H E C S Q I S A 617 V A H E C S R V P S 618 V A H E C S R V P A 619 V A H E C S R V S S 620 V A H E C S R V S A 621 V A H E C S R I P S 622 V A H E C S R I P A 623 V A H E C S R I S S 624 V A H E C S R I S A 625 V A H E C P Q V P S 626 V A H E C P Q V P A 627 V A H E C P Q V S S 628 V A H E C P Q V S A 629 V A H E C P Q I P S 630 V A H E C P Q I P A 631 V A H E C P C I S S 632 V A H E C P Q I S A 633 V A H E C P R V P S 634 V A H E C P R V P A 635 V A H E C P R V S S 636 V A H E C P R V S A 637 V A H E C P R I P S 638 V A H E C P R I P A 639 V A H E C P R I S S 640 V A H E C P R I S A 641 V A H E R S Q V P S 642 V A H E R S Q V P A 643 V A H E R S Q V S S 644 V A H E R S Q V S A 645 V A H E R S Q I P S 646 V A H E R S Q I P A 647 V A H E R S Q I S S 648 V A H E R S Q I S A 649 V A H E R S R V P S 650 V A H E R S R V P A 651 V A H E R S R V S S 652 V A H E R S R V S A 653 V A H E R S R I P S 654 V A H E R S R I P A 655 V A H E R S R I S S 656 V A H E R S R I S A 657 V A H E R P Q V P S 658 V A H E R P Q V P A 659 V A H E R P Q V S S 660 V A H E R P Q V S A 661 V A H E R P Q I P S 662 V A H E R P Q I P A 663 V A H E R P Q I S S 664 V A H E R P Q I S A 665 V A H E R P R V P S 666 V A H E R P R V P A 667 V A H E R P R V S S 668 V A H E R P R V S A 669 V A H F R P R I P S 670 V A H E R P R I P A 671 V A H F R P R I S S 672 V A H E R P R I S A 673 V A H A C S Q V P S 674 V A H A C S Q V P A 675 V A H A C S Q V S S 676 V A H A C S Q V S A 677 V A H A C S Q I P S 678 V A H A C S Q I P A 679 V A H A C S Q I S S 680 V A H A C S Q I S A 681 V A H A C S R V P S 682 V A H A C S R V P A 683 V A H A C S R V S S 684 V A H A C S R V S A 685 V A H A C S R I P S 686 V A H A C S R I P A 687 V A H A C S R I S S 688 V A H A C S R I S A 689 V A H A C P Q V P S 690 V A H A C P Q V P A 691 V A H A C P Q V S S 692 V A H A C P Q V S A 693 V A H A C P Q I P S 694 V A H A C P Q I P A 695 V A H A C P Q I S S 696 V A H A C P Q I S A 697 V A H A C P R V P S 698 V A H A C P R V P A 699 V A H A C P R V S S 700 V A H A C P R V S A 701 V A H A C P R I P S 702 V A H A C P R I P A 703 V A H A C P R I S S 704 V A H A C P R I S A 705 V A H A R S Q V P S 706 V A H A R S Q V P A 707 V A H A R S Q V S S 708 V A H A R S Q V S A 709 V A H A R S Q I P S 710 V A H A R S Q I P A 711 V A H A R S Q I S S 712 V A H A R S Q I S A 713 V A H A R S R V P S 714 V A H A R S R V P A 715 V A H A R S R V S S 716 V A H A R S R V S A 717 V A H A R S R I P S 718 V A H A R S R I P A 719 V A H A R S R I S S 720 V A H A R S R I S A 721 V A H A R P Q V P S 722 V A H A R P Q V P A 723 V A H A R P Q V S S 724 V A H A R P Q V S A 725 V A H A R P Q I P S 726 V A H A R P Q I P A 727 V A H A R P Q I S S 728 V A H A R P Q I S A 729 V A H A R P R V P S 730 V A H A R P R V P A 731 V A H A R P R V S S 732 V A H A R P R V S A 733 V A H A R P R I P S 734 V A H A R P R I P A 735 V A H A R P R I S S 736 V A H A R P R I S A 737 V T R E C S Q V P S 738 V T R E C S Q V P A 739 V T R E C S Q V S S 740 V T R E C S Q V S A 741 V T R E C S Q I P S 742 V T R E C S Q I P A 743 V T R E C S Q I S S 744 V T R E C S Q V S A 745 V T R E C S R V P S 746 V T R E C S R V P A 747 V T R E C S R V S S 748 V T R F C S R V S A 749 V T R E C S R I P S 750 V T R E C S R I P A 751 V T R E C S R I S S 752 V T R E C S R I S A 753 V T R E C P Q V P S 754 V T R E C P Q V P A 755 V T R E C P Q V S S 756 V T R E C P Q V S A 757 V T R F C P Q I P S 758 V T R E C P Q I P A 759 V T R E C P Q I S S 760 V T R E C P Q I S A 761 V T R E C P R V P S 762 V T R E C P R V P A 763 V T R F C P R V S S 764 V T R E C P R V S A 765 V T R E C P R I P S 766 V T R F C P R I P A 767 V T R E C P R I S S 768 V T R E C P R I S A 769 V T R E R S Q V P S 770 V T R E R S Q V P A 771 V T R E R S Q V S S 772 V T R E R S Q V S A 773 V T R E R S Q I P S 774 V T R E R S Q I P A 775 V T R E R S Q I S S 776 V T R E R S Q I S A 777 V T R E R S R V P S 778 V T R E R S R V P A 779 V T R F R S R V S S 780 V T R E R S R V S A 781 V T R E R S R I P S 782 V T R E R S R I P A 783 V T R E R S R I S S 784 V T R E R S R I S A 785 V T R E R P Q V P S 786 V T R E R P Q V P A 787 V T R E R P Q V S S 788 V T R E R P Q V S A 789 V T R E R P Q I P S 790 V T R E R P Q I P A 791 V T R F R P Q I S S 792 V T R E R P Q I S A 793 V T R E R P R V P S 794 V T R F R P R V P A 795 V T R E R P R V S S 796 V T R E R P R V S A 797 V T R E R P R I P S 798 V T R E R P R I P A 799 V T R E R P R I S S 800 V T R E R P R I S A 801 V T R A C S Q V P S 802 V T R A C S Q V P A 803 V T R A C S Q V S S 804 V T R A C S Q V S A 805 V T R A C S Q I P S 806 V T R A C S Q I P A 807 V T R A C S Q I S S 808 V T R A C S Q I S A 809 V T R A C S R V P S 810 V T R A C S R V P A 811 V T R A C S R V S S 812 V T R A C S R V S A 813 V T R A C S R I P S 814 V T R A C S R I P A 815 V T R A C S R I S S 816 V T R A C S R I S A 817 V T R A C P Q V P S 818 V T R A C P Q V P A 819 V T R A C P Q V S S 820 V T R A C P Q V S A 821 V T R A C P Q I P S 822 V T R A C P Q I P A 823 V T R A C P Q I S S 824 V i R A C P Q I S A 825 V T R A C P R V P S 826 V T R A C P R V P A 827 V T R A C P R V S S 828 V T R A C P R V S A 829 V T R A C P R I P S 830 V T R A C P R I P A 831 V T R A C P R I S S 832 V T R A C P R I S A 833 V T R A R S Q V P S 834 V T R A R S Q V P A 835 V T R A R S Q V S S 836 V T R A R S Q V S A 837 V T R A R S Q I P S 838 V T R A R S Q I P A 839 V T R A R S Q I S S 840 V T R A R S Q I S A 841 V T R A R S R V P S 842 V T R A R S R V P A 843 V T R A R S R V S S 844 V T R A R S R V S A 845 V T R A R S R I P S 846 V T R A R S R I P A 847 V T R A R S R I S S 848 V T R A R S R I S A 849 V T R A R P Q V P S 850 V T R A R P Q V P A 851 V T R A R P Q V S S 852 V T R A R P Q V S A 853 V T R A R P Q I P S 854 V T R A R P Q I P A 855 V T R A R P Q I S S 856 V T R A R P Q I S A 857 V T R A R P R V P S 858 V T R A R P R V P A 859 V T R A R P R V S S 860 V T R A R P R V S A 861 V T R A R P R I P S 862 V T R A R P R I P A 863 V T R A R P R I S S 864 V T R A R P R I S A 865 V T H F C S Q V P S 866 V T H F C S Q V P A 867 V T H E C S Q V S S 868 V T H E C S Q V S A 869 V T H E C S Q I P S 870 V T H E C S Q I P A 871 V T H E C S Q I S S 872 V T H E C S Q I S A 873 V T H E C S R V P S 874 V T H E C S R V P A 875 V T H E C S R V S S 876 V T H E C S R V S A 877 V T H E C S R I P S 878 V T H E C S R I P A 879 V T H E C S R I S S 880 V T H F C S R I S A 881 V T H E C P Q V P S 882 V T H E C P Q V P A 883 V T H F C P Q V S S 884 V T H E C P Q V S A 885 V T H E C P Q I P S 886 V T H E C P Q I P A 887 V T H E C P Q I S S 888 V T H E C P Q I S A 889 V T H F C P R V P S 890 V T H F C P R V P A 891 V T H E C P R V S S 892 V T H E C P R V S A 893 V T H E C P R I P S 894 V T H E C P R I P A 895 V T H E C P R I S S 896 V T H E C P R I S A 897 V T H E R S Q V P S 898 V T H E R S Q V P A 899 V T H E R S Q V S S 900 V T H E R S Q V S A 901 V T H E R S Q I P S 902 V T H E R S Q I P A 903 V T H E R S Q I S S 904 V T H E R S Q I S A 905 V T H E R S R V P S 906 V T H E R S R V P A 907 V T H E R S R V S S 908 V T H E R S R V S A 909 V T H E R S R I P S 910 V T H E R S R I P A 911 V T H E R S R I S S 912 V T H E R S R I S A 913 V T H E R P Q V P S 914 V T H E R P Q V P A 915 V T H E R P Q V S S 916 V T H E R P Q V S A 917 V T H E R P Q I P S 918 V T H E R P Q I P A 919 V T H E R P Q I S S 920 V T H E R P Q I S A 921 V T H E R P R V P S 922 V T H E R P R V P A 923 V T H E R P R V S S 924 V T H E R P R V S A 925 V T H E R P R I P S 926 V T H E R P R I P A 927 V T H E R P R I S S 928 V T H E R P R I S A 929 V T H A C S Q V P S 930 V T H A C S Q V P A 931 V T H A C S Q V S S 932 V T H A C S Q V S A 933 V T H A C S Q I P S 934 V T H A C S Q I P A 935 V T H A C S Q I S S 936 V T H A C S Q I S A 937 V T H A C S R V P S 938 V T H A C S R V P A 939 V T H A C S R V S S 940 V T H A C S R V S A 941 V T H A C S R I P S 942 V T H A C S R I P A 943 V T H A C S R I S S 944 V T H A C S R I S A 945 V T H A C P Q V P S 946 V T H A C P Q V P A 947 V T H A C P Q V S S 948 V T H A C P Q V S A 949 V T H A C P Q I P S 950 V T H A C P Q I P A 951 V T H A C P Q I S S 952 V T H A C P Q I S A 953 V T H A C P R V P S 954 V T H A C P R V P A 955 V T H A C P R V S S 956 V T H A C P R V S A 957 V T H A C P R I P S 958 V T H A C P R I P A 959 V T H A C P R I S S 960 V T H A C P R I S A 961 V T H A R S Q V P S 962 V T H A R S Q V P A 963 V T H A R S Q V S S 964 V T H A R S Q V S A 965 V T H A R S Q I P S 966 V T H A R S Q I P A 967 V T H A R S Q I S S 968 V T H A R S Q I S A 969 V T H A R S R V P S 970 V T H A R S R V P A 971 V T H A R 3 R V S S 972 V T H A R S R V S A 973 V T H A R S R I P S 974 V T H A R S R I P A 975 V T H A R S R I S S 976 V T H A R S R I S A 977 V T H A R P Q V P S 978 V T H A R P Q V P A 979 V T H A R P Q V S S 980 V T H A R P Q V S A 981 V T H A R P Q I P S 982 V T H A R P Q I P A 983 V T H A R P Q I S S 984 V T H A R P Q I S A 985 V T H A R P R V P S 986 V T H A R P R V P A 987 V T H A R P R V S S 988 V T H A R P R V S A 989 V T H A R P R I P S 990 V T H A R P R I P A 991 V T H A R P R I S S 992 V T H A R P R I S A

[0081] The invention also includes IL4Rα peptide variants, which are any fragments of an IL4Rα protein variant that contains one or more of the amino acid variations shown in Table 2. An IL4Rα peptide variant is at least 6 amino acids in length and is preferably any number between 6 and 30 amino acids long, more preferably between 10 and 25, and most preferably between 15 and 20 amino acids long. Such IL4Rα peptide variants may be useful as antigens to generate antibodies specific for one of the above IL4Rα isoforms. In addition, the IL4Rα peptide variants may be useful in drug screening

[0082] An IL4Rα variant protein or peptide of the invention may be prepared by chemical synthesis or by expressing one of the variant IL4Rα genomic and cDNA sequences as described above. Alternatively, the IL4Rα protein variant may be isolated from a biological sample of an individual having an IL4Rα isogene which encodes the variant protein. Where the sample contains two different IL4Rα isoforms (i.e., the individual has different IL4Rα isogenes), a particular IL4Rα isoform of the invention can be isolated by immunoaffinity chromatography using an antibody which specifically binds to that particular IL4Rα isoform but does not bind to the other IL4Rα isoform.

[0083] The expressed or isolated IL4Rα protein may be detected by methods known in the art, including Coomassie blue staining, silver staining, and Western blot analysis using antibodies specific for the isoform of the IL4Rα protein as discussed further below. IL4Rα variant proteins can be purified by standard protein purification procedures known in the art, including differential precipitation, molecular sieve chromatography, ion-exchange chromatography, isoelectric focusing, gel electrophoresis, affinity and immunoaffinity chromatography and the like. (Ausubel et. al., 1987, In Current Protocols in Molecular Biology John Wiley and Sons, New York, N.Y.). In the case of immunoaffinity chromatography, antibodies specific for a particular polymorphic variant may be used.

[0084] A polymorphic variant IL4Rα gene of the invention may also be fused in frame with a heterologous sequence to encode a chimeric IL4Rα protein. The non-IL4Rα portion of the chimeric protein may be recognized by a commercially available antibody. In addition, the chimeric protein may also be engineered to contain a cleavage site located between the IL4Rα and non-IL4Rα portions so that the IL4Rα protein may be cleaved and purified away from the non-IL4Rα portion.

[0085] An additional embodiment of the invention relates to using a novel IL4Rα protein isoform in any of a variety of drug screening assays. Such screening assays may be performed to identify agents that bind specifically to all known IL4Rα protein isoforms or to only a subset of one or more of these isoforms. The agents may be from chemical compound libraries, peptide libraries and the like. The IL4Rα protein or peptide variant may be free in solution or affixed to a solid support. In one embodiment, high throughput screening of compounds for binding to an IL4Rα variant may be accomplished using the method described in PCT application WO84/03565, in which large numbers of test compounds are synthesized on a solid substrate, such as plastic pins or some other surface, contacted with the IL4Rα protein(s) of interest and then washed. Bound IL4Rα protein(s) are then detected using methods well-known in the art.

[0086] In another embodiment, a novel IL4Rα protein isoform may be used in assays to measure the binding affinities of one or more candidate drugs targeting the IL4Rα protein.

[0087] In another embodiment, the invention provides antibodies specific for and immunoreactive with one or more of the novel IL4Rα variant proteins described herein. The antibodies may be either monoclonal or polyclonal in origin. The IL4Rα protein or peptide variant used to generate the antibodies may be from natural or recombinant sources or produced by chemical synthesis using synthesis techniques known in the art. If the IL4Rα protein variant is of insufficient size to be antigenic, it may be conjugated, complexed, or otherwise covalently linked to a carrier molecule to enhance the antigenicity of the peptide. Examples of carrier molecules, include, but are not limited to, albumins (e.g., human, bovine, fish, ovine), and keyhole limpet hemocyanin (Basic and Clinical Immunology, 1991, Eds. D. P. Stites, and A. I. Terr, Appleton and Lange, Norwalk Conn., San Mateo, Calif.).

[0088] In one embodiment, an antibody specifically immunoreactive with one of the novel IL4Rα protein isoforms described herein is administered to an individual to neutralize activity of the IL4Rα isoform expressed by that individual. The antibody may be formulated as a pharmaceutical composition which includes a pharmaceutically acceptable carrier.

[0089] Antibodies specific for and immunoreactive with one of the novel IL4Rα protein isoform described herein may be used to immunoprecipitate the IL4Rα protein variant from solution as well as react with IL4Rα protein isoforms on Western or immunoblots of polyacrylamide gels on membrane supports or substrates. In another preferred embodiment, the antibodies will detect IL4Rα protein isoforms in paraffin or frozen tissue sections, or in cells which have been fixed or unfixed and prepared on slides, coverslips, or the like, for use in immunocytochemical, immunohistochemical, and immunofluorescence techniques.

[0090] In another embodiment, an antibody specifically immunoreactive with one of the novel IL4Rα protein variants described herein is used in immunoassays to detect this variant in biological samples. In this method, an antibody of the present invention is contacted with a biological sample and the formation of a complex between the IL4Rα protein variant and the antibody is detected. As described, suitable immunoassays include radioimmunoassay, Western blot assay, immunofluorescent assay, enzyme linked immunoassay (ELISA), chemiluminescent assay, immunohistochemical assay, immunocytochemical assay, and the like (see, e.g., Principles and Practice of Immunoassay, 1991, Eds. Christopher P. Price and David J. Neoman, Stockton Press, New York, N.Y.; Current Protocols in Molecular Biology, 1987, Eds. Ausubel et al., John Wiley and Sons, New York, N.Y.). Standard techniques known in the art for ELISA are described in Methods in Immunodiagnosis, 2nd Ed., Eds. Rose and Bigazzi, John Wiley and Sons, New York 1980; and Campbell et al., 1984, Methods in Immunology, W. A. Benjamin, Inc.). Such assays may be direct, indirect, competitive, or noncompetitive as described in the art (see, e.g., Principles and Practice of Immunoassay, 1991, Eds. Christopher P. Price and David J. Neoman, Stockton Pres, NY, N.Y.; and Oellirich, M., 1984, J. Clin. Chem. Clin. Biochem., 22:895-904). Proteins may be isolated from test specimens and biological samples by conventional methods, as described in Current Protocols in Molecular Biology, supra.

[0091] Exemplary antibody molecules for use in the detection and therapy methods of the present invention are intact immunoglobulin molecules, substantially intact inununoglobulin molecules, or those portions of immunoglobulin molecules that contain the antigen binding site. Polyclonal or monoclonal antibodies may be produced by methods conventionally known in the art (e.g., Kohler and Milstein, 1975, Nature, 256:495-497; Campbell Monoclonal Antibody Technology, the Production and Characterization of Rodent and Human Hybridomas, 1985, In: Laboratory Techniques in Biochemistry and Molecular Biology, Eds. Burdon et al., Volume 13, Elsevier Science Publishers, Amsterdam). The antibodies or antigen binding fragments thereof may also be produced by genetic engineering. The technology for expression of both heavy and light chain genes in E. coli is the subject of PCT patent applications, publication number WO 901443, WO 901443 and WO 9014424 and in Huse et al., 1989, Science, 246:1275-1281. The antibodies may also be humanized (e.g., Queen, C. et al. 1989 Proc. Natl. Acad. Sci. 86;10029).

[0092] Effect(s) of the polymorphisms identified herein on expression of IL4Rα may be investigated by preparing recombinant cells and/or organisms, preferably recombinant animals, containing a polymorphic variant of the IL4Rα gene. As used herein, “expression” includes but is not limited to one or more of the following: transcription of the gene into precursor mRNA; splicing and other processing of the precursor mRNA to produce mature mRNA; mRNA stability; translation of the mature mRNA into IL4Rα protein (including codon usage and tRNA availability); and glycosylation and/or other modifications of the translation product, if required for proper expression and function.

[0093] To prepare a recombinant cell of the invention, the desired IL4Rα isogene may be introduced into the cell in a vector such that the isogene remains extrachromosomal. In such a situation, the gene will be expressed by the cell from the extrachromosomal location. In a preferred embodiment, the IL4Rα isogene is introduced into a cell in such a way that it recombines with the endogenous IL4Rα gene present in the cell. Such recombination requires the occurrence of a double recombination event, thereby resulting in the desired IL4Rα gene polymorphism. Vectors for the introduction of genes both for recombination and for extrachromosomal maintenance are known in the art, and any suitable vector or vector construct may be used in the invention. Methods such as electroporation, particle bombardment, calcium phosphate co-precipitation and viral transduction for introducing DNA into cells are known in the art; therefore, the choice of method may lie with the competence and preference of the skilled practitioner. Examples of cells into which the IL4Rα isogene may be introduced include, but are not limited to, continuous culture cells, such as COS, NIH/3T3, and primary or culture cells of the relevant tissue type, i.e., they express the IL4Rα isogene. Such recombinant cells can be used to compare the biological activities of the different protein variants.

[0094] Recombinant organisms, i.e., transgenic animals, expressing a variant IL4Rα gene are prepared using standard procedures known in the art. Preferably, a construct comprising the variant gene is introduced into a nonhuman animal or an ancestor of the animal at an embryonic stage, i.e., the one-cell stage, or generally not later than about the eight-cell stage. Transgenic animals carrying the constructs of the invention can be made by several methods known to those having skill in the art. One method involves transfecting into the embryo a retrovirus constructed to contain one or more insulator elements, a gene or genes of interest, and other components known to those skilled in the art to provide a complete shuttle vector harboring the insulated gene(s) as a transgene, see e.g., U.S. Pat. No. 5,610,053. Another method involves directly injecting a transgene into the embryo. A third method involves the use of embryonic stem cells. Examples of animals into which the IL4Rα isogenes may be introduced include, but are not limited to, mice, rats, other rodents, and nonhuman primates (see “The Introduction of Foreign Genes into Mice” and the cited references therein, In: Recombinant DNA, Eds. J. D. Watson, M. Gilman, J. Witkowski, and M. Zoller; W. H. Freeman and Company, New York, pages 254-272). Transgenic animals stably expressing a human IL4Rα isogene and producing human IL4Rα protein can be used as biological models for studying diseases related to abnormal IL4Rα expression and/or activity, and for screening and assaying various candidate drugs, compounds, and treatment regimens to reduce the symptoms or effects of these diseases.

[0095] An additional embodiment of the invention relates to pharmaceutical compositions for treating disorders affected by expression or function of a novel IL4Rα isogene described herein. The pharmaceutical composition may comprise any of the following active ingredients: a polynucleotide comprising one of these novel IL4Rα isogenes; an antisense oligonucleotide directed against one of the novel IL4Rα isogenes, a polynucleotide encoding such an antisense oligonucleotide, or another compound which inhibits expression of a novel IL4Rα isogene described herein. Preferably, the composition contains the active ingredient in a therapeutically effective amount. By therapeutically effective amount is meant that one or more of the symptoms relating to disorders affected by expression or function of a novel IL4Rα isogene is reduced and/or eliminated. The composition also comprises a pharmaceutically acceptable carrier, examples of which include, but are not limited to, saline, buffered saline, dextrose, and water. Those skilled in the art may employ a formulation most suitable for the active ingredient, whether it is a polynucleotide, oligonucleotide, protein, peptide or small molecule antagonist. The pharmaceutical composition may be administered alone or in combination with at least one other agent, such as a stabilizing compound. Administration of the pharmaceutical composition may be by any number of routes including, but not limited to oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, intradermal, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, or rectal. Further details on techniques for formulation and administration may be found in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing Co., Easton, Pa.).

[0096] For any composition, determination of the therapeutically effective dose of active ingredient and/or the appropriate route of administration is well within the capability of those skilled in the art. For example, the dose can be estimated initially either in cell culture assays or in animal models. The animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans. The exact dosage will be determined by the practitioner, in light of factors relating to the patient requiring treatment, including but not limited to severity of the disease state, general health, age, weight and gender of the patient, diet, time and frequency of administration, other drugs being taken by the patient, and tolerance/response to the treatment.

[0097] Information on the identity of genotypes and haplotypes for the IL4Rα gene of any particular individual as well as the frequency of such genotypes and haplotypes in any particular population of individuals is expected to be useful for a variety of basic research and clinical applications. Thus, the invention also provides compositions and methods for detecting the novel IL4Rα polymorphisms identified herein.

[0098] The compositions comprise at least one IL4Rα genotyping oligonucleotide. In one embodiment, an IL4Rα genotyping oligonucleotide is a probe or primer capable of hybridizing to a target region that is located close to, or that contains, one of the novel polymorphic sites described herein. As used herein, the term “oligonucleotide” refers to a polynucleotide molecule having less than about 100 nucleotides. A preferred oligonucleotide of the invention is 10 to 35 nucleotides long. More preferably, the oligonucleotide is between 15 and 30, and most preferably, between 20 and 25 nucleotides in length. The oligonucleotide may be comprised of any phosphorylation state of ribonucleotides, deoxyribonucleotides, and acyclic nucleotide derivatives, and other functionally equivalent derivatives. Alternatively, oligonucleotides may have a phosphate-free backbone, which may be comprised of linkages such as carboxymethyl, acetamidate, carbamate, polyamide (peptide nucleic acid (PNA)) and the like (Varma, R. in Molecular Biology and Biotechnology, A Comprehensive Desk Reference, Ed. R. Meyers, VCH Publishers, Inc. (1995), pages 617-620). Oligonucleotides of the invention may be prepared by chemical synthesis using any suitable methodology known in the art, or may be derived from a biological sample, for example, by restriction digestion. The oligonucleotides may be labeled, according to any technique known in the art, including use of radiolabels, fluorescent labels, enzymatic labels, proteins, haptens, antibodies, sequence tags and the like.

[0099] Genotyping oligonucleotides of the invention must be capable of specifically hybridizing to a target region of an IL4Rα polynucleotide, i.e., an IL4Rα isogene. As used herein, specific hybridization means the oligonucleotide forms an anti-parallel double-stranded structure with the target region under certain hybridizing conditions, while failing to form such a structure when incubated with a non-target region or a non-IL4Rα polynucleotide under the same hybridizing conditions. Preferably, the oligonucleotide specifically hybridizes to the target region under conventional high stringency conditions. The skilled artisan can readily design and test oligonucleotide probes and primers suitable for detecting polymorphisms in the IL4Rα gene using the polymorphism information provided herein in conjunction with the known sequence information for the IL4Rα gene and routine techniques.

[0100] A nucleic acid molecule such as an oligonucleotide or polynucleotide is said to be a “perfect” or “complete” complement of another nucleic acid molecule if every nucleotide of one of the molecules is complementary to the nucleotide at the corresponding position of the other molecule. A nucleic acid molecule is “substantially complementary” to another molecule if it hybridizes to that molecule with sufficient stability to remain in a duplex form under conventional low-stringency conditions. Conventional hybridization conditions are described, for example, by Sambrook J. et al., in Molecular Cloning, A Laboratory Manual, 2^(nd) Edition, Cold Spring Harbor Press, Cold Spring Harbor, NY (1989) and by Haymes, B. D. et al. in Nucleic Acid Hybridization, A Practical Approach, IRL Press, Washington, D.C. (1985). While perfectly complementary oligonucleotides are preferred for detecting polymorphisms, departures from complete complementarity are contemplated where such departures do not prevent the molecule from specifically hybridizing to the target region. For example, an oligonucleotide primer may have a non-complementary fragment at its 5′ end, with the remainder of the primer being complementary to the target region. Alternatively, non-complementary nucleotides may be interspersed into the oligonucleotide probe or primer as long as the resulting probe or primer is still capable of specifically hybridizing to the target region.

[0101] Preferred genotyping oligonucleotides of the invention are allele-specific oligonucleotides. As used herein, the term allele-specific oligonucleotide (ASO) means an oligonucleotide that is able, under sufficiently stringent conditions, to hybridize specifically to one allele of a gene, or other locus, at a target region containing a polymorphic site while not hybridizing to the corresponding region in another allele(s). As understood by the skilled artisan, allele-specificity will depend upon a variety of readily optimized stringency conditions, including salt and formamide concentrations, as well as temperatures for both the hybridization and washing steps. Examples of hybridization and washing conditions typically used for ASO probes are found in Kogan et al., “Genetic Prediction of Hemophilia A” in PCR Protocols, A Guide to Methods and Applications, Academic Press, 1990 and Ruano et al., 87 Proc. Natl. Acad. Sci. USA 6296-6300, 1990. Typically, an allele-specific oligonucleotide will be perfectly complementary to one allele while containing a single mismatch for another allele.

[0102] Allele-specific oligonucleotide probes which usually provide good discrimination between different alleles are those in which a central position of the oligonucleotide probe aligns with the polymorphic site in the target region (e.g., approximately the 7^(th) or 8^(th) position in a 15 mer, the 8^(th) or 9^(th) position in a 16mer, the 10^(th) or 11 ^(th) position in a 20 mer). A preferred ASO probe for detecting IL4Rα gene polymorphisms comprises a nucleotide sequence, listed 5′ to 3′, selected from the group consisting of: TTGCACCACTGCACT and its complement, (SEQ ID NO:4) TTGCACCGCTGCACT and its complement, (SEQ ID NO:5) TTTTGTGCTATTCCC and its complement, (SEQ ID NO:6) TTTTGTGTTATTCCC and its complement, (SEQ ID NO:7) CTGGGCCGCTCAGGC and its complement, (SEQ ID NO:8) CTGGGCCTCTCAGGC and its complement, (SEQ ID NO:9) TAAGCCTGCGCTGGA and its complement, (SEQ ID NO:10) TAAGCCTCCGCTGGA and its complement, (SEQ ID NO:11) AGAACAACGGAGGCG and its complement, (SEQ ID NO:12) AGAACAATGGAGGCG and its complement, (SEQ ID NO:13) CGGAGGCGCGGGGTG and its complement, (SEQ ID NO:14) CGGAGGCACGGGGTG and its complement, (SEQ ID NO:15) GTGCGGATAACTATA and its complement, (SEQ ID NO:16) GTGCGGACAACTATA and its complement, (SEQ ID NO:17) CGGAGTGCGGCAGGG and its complement, (SEQ ID NO:18) CGGAGTGTGGCAGGG and its complement, (SEQ ID NO:19) GCCTGGGCTGAGGGT and its complement, (SEQ ID NO:20) GCCTGGGTTGAGGGT and its complement, (SEQ ID NO:21) TGGGGTGGGCAGGGG and its complement, (SEQ ID NO:22) TGGGGTGAGCAGGGG and its complement, (SEQ ID NO:23) TTCTCCCGCAGTGAA and its complement, (SEQ ID NO:24) TTCTCCCACAGTGAA and its complement, (SEQ ID NO:25) GTGAAAACGACCCGG and its complement, (SEQ ID NO:26) GTGAAAATGACCCGG and its complement, (SEQ ID ND:27) GGCAAGCCCTGGGGC and its complement, (SEQ ID NO:28) GGCAAGCTCTGGGGC and its complement, (SEQ ID NO:29) GCCCTGGGGCTGGAT and its complement, (SEQ ID NO:30) GCCCTGGAGCTGGAT and its complement, (SEQ ID NO:31) ATAGCAAATCCCAGG and its complement, (SEQ ID NO:32) ATAGCAATTCCCAGG and its complement, (SEQ ID NO:33) GCTCTGCCCTAGGCA and its complement, (SEQ ID NO:34) GCTCTGCACTAGGCA and its complement, (SEQ ID NO:35) CCCCCACCCCTCACA and its complement, (SEQ ID NO:36) CCCOCACTCCTCACA and its complement, (SEQ ID NO:37) TCCCTCCGCATCGCA and its complement, (SEQ ID NO:38) TCCCTCCACATCGCA and its complement, (SEQ ID NO:39) CACCTGCTGTGGTGT and its complement, (SEQ ID NO:40) CACCTGCCGTGGTGT and its complement, (SEQ ID NO:41) ATGTCTGAAGTAGAC and its complement, (SEQ ID NO:42) ATGTCTGCAGTAGAC and its complement, (SEQ ID NO:43) TGACCAACCTTTGCT and its complement, (SEQ ID NO:44) TGACCAACTTTTGCT and its complement, (SEQ ID NO:45) CCTGTTTTCTGGAGC and its complement, (SEQ ID NO:46) CCTGTTTCCTGGAGC and its complement, (SEQ ID NO:47) TGGAGCTGCTCGGAG and its complement, (SEQ ID NO:48) TGGACCTTCTCGGAG and its complement, (SEQ ID NO:49) AGTCATGCCTTCTTC and its complement, (SEQ ID NO:50) AGTCATGTCTTCTTC and its complement, (SEQ ID NO:51) GCCTTCTTCCACCTT and its complement, (SEQ ID NO:52) GCCTTCTCCCACCTT and its complement, (SEQ ID NO:53) CAGCCCCCGTCTCGG and its complement, (SEQ ID NO:54) CAGCCCCTGTCTCGG and its complement, (SEQ ID NO:55) GGAGTTTGTACATGC and its complement, (SEQ ID NO:56) GGAGTTTATACATGC and its complement, (SEQ ID NO:57) CAGCTCCCCAGAGCA and its complement, (SEQ ID NO:58) CAGCTCCTCAGAGCA and its complement, (SEQ ID NO:59) AGACAGGTCCTCGCC and its complement, (SEQ ID NO:60) AGACAGGGCCTCGCC and its complement, (SEQ ID NO:61) CTGCCCCTGGCAATG and its complement, (SEQ ID NO:62) CTGCCCCCGGCAATG and its complement, (SEQ ID NO:63) AGGTGCATGTCCTCT and its complement, (SEQ ID NO:64) AGGTGCACGTCCTCT and its complement, (SEQ ID NO:65) GTGCATGTCCTCTTG and its complement, (SEQ ID NO:66) GTGCATGCCCTCTTG and its complement, (SEQ ID NO:67) GGCTTATCCATGCCT and its complement, (SEQ ID NO:68) GGCTTATTCATGCCT and its complement, (SEQ ID NO:69) AGCCAGGCTGGCAGA and its complement, (SEQ ID NO:70) AGCCAGGGTGGCAGA and its complement, (SEQ ID NO:71) GGCCGACATGGAGGC and its complement, (SEQ ID NO:72) GGCCCACGTGGAGGC and its complement, (SEQ ID NO:73) TAACACAGCCATCAA and its complement, (SEQ ID NO:74) TAACACAACCATCAA and its complement, (SEQ ID NO:75) TAATGCTCGTCTGTG and its complement, (SEQ ID NO:76) TAATGCTTGTCTGTG and its complement, (SEQ ID NO:77) ACTTGCCGTCTGGGT and its complement, (SEQ ID NO:78) and ACTTGCCATCTGGGT and its complement. (SEQ ID NO:79)

[0103] An allele-specific oligonucleotide primer of the invention has a 3′ terminal nucleotide, or preferably a 3′ penultimate nucleotide, that is complementary to only one nucleotide of a particular SNP, thereby acting as a primer for polymerase-mediated extension only if the allele containing that nucleotide is present. Allele-specific oligonucleotide primers hybridizing to either the coding or noncoding strand are contemplated by the invention. A preferred ASO primer for detecting IL4Rα gene polymorphisms comprises a nucleotide sequence, listed 5′ to 3′, selected from the group consisting of: CTGAGATTGCACCAC; (SEQ ID NO:80) GGCTGGAGTGCAGTG; (SEQ ID NO:81) CTGAGATTGCACCGC; (SEQ ID NO:82) GCCTGGAGTGCAGCG; (SEQ ID NO:83) CTGTGCTTTTGTGCT; (SEQ ID NO:84) ACCAAGGGGAATAGC; (SEQ ID NO:85) CTGTGCTTTTGTGTT; (SEQ ID NO:86) ACCAAGGGGAATAAC; (SEQ ID NO:87) GAGTTCCTGGGCCGC; (SEQ ID NO:88) GGAGCAGCCTGAGCG; (SEQ ID NO:89) GAGTTCCTGGGCCTC; (SEQ ID NO:90) GGAGCAGCCTGAGAG; (SEQ ID NO:91) TCCGAGTAAGCCTGC; (SEQ ID NO:92) TCCAGCTCCAGCGCA; (SEQ ID NO:93) TCCGAGTAAGCCTCC; (SEQ ID NO:94) TCCAGCTCCAGCGGA; (SEQ ID NO:95) TCCCTGAGAACAACG; (SEQ ID NO:96) ACCCCGCGCCTCCGT; (SEQ ID NO:97) TCCCTGAGAACAATG; (SEQ ID NO:98) ACCCCGCGCCTCCAT; (SEQ ID NQ:99) GAACAACGGAGGCGC; (SEQ ID NO:100) CACACGCACCCCGCG; (SEQ ID NO:101) GAACAACGGAGGCAC; (SEQ ID NO:102) CACACGCACCCCGTG; (SEQ ID NO:103) TGGTCAGTGCGGATA; (SEQ ID NO:104) CCAGTGTATAGTTAT; (SEQ ID NO:105) TGGTCAGTGCGGACA; (SEQ ID NO:106) CCAGTGTATAGTTGT; (SEQ TD NO:107) GCAGGGCGGAGTGCG; (SEQ ID NO:108) AGCCACCCCTGCCGC; (SEQ ID NO:109) GCAGGGCGGAGTGTG; (SEQ ID NO:110) AGCCACCCCTGCCAC; (SEQ ID NO:111) ACAGCTGCCTGGGCT; (SEQ ID NO:112) CACCGCACCCTCAGC; (SEQ ID NO:113) ACAGCTGCCTGGGTT; (SEQ ID NO:114) CACCCCACCCTCAAC; (SEQ ID NO:115) TGAGGGTGGGGTGGG; (SEQ ID NO:116) CCTCCTCCCCTGCCC; (SEQ ID NO:117) TGAGGGTGGGGTGAG; (SEQ ID NO:118) CCTCCTCCCCTGCTC; (SEQ ID NO:119) GGCCGCTTCTCCCGC; (SEQ ID NO:120) CTGGGTTTCACTGCG; (SEQ ID NO:121) GGCCGCTTCTCCCAC; (SEQ ID NO:122) CTGGGTTTCACTGTG; (SEQ ID NO:123) TTTGGAGTGAAAACG; (SEQ ID NO:124) CATCTGCCGGGTCGT; (SEQ ID NO:125) TTTGGAGTGAAAATG; (SEQ ID NO:126) CATCTGCCGGGTCAT; (SEQ ID NO:127) CTGGGAGGCAAGCCC; (SEQ ID NO:128) TATCCAGCCCCAGGG; (SEQ ID NO:129) CTGGGAGGCAAGCTC; (SEQ ID NO:130) TATCCAGCCOCAGAG; (SEQ ID NO:131) AGGCAAGCCCTGGGG; (SEQ ID NO:132) TTTGCTATCCAGCCC; (SEQ ID NO:133) AGGCAAGCCCTGGAG; (SEQ ID NO:134) TTTGCTATCCAGCTC; (SEQ ID NO:135) GGCTGGATAGCAAAT; (SEQ ID NO:136) CTAGCTCCTGGGATT; (SEQ ID NO:137) GGCTGGATAGCAATT; (SEQ ID NQ:138) CTAGCTCCTGGGAAT; (SEQ ID NO:139) CACCTGGCTCTGCCC; (SEQ ID NO:140) GGGACTTGCCTAGGG; (SEQ ID NO:141) CACCTGGCTCTGCAC; (SEQ ID NO:142) GGGACTTGCCTAGTG; (SEQ ID NO:143) CCTGGCCCCCCACCC; (SEQ ID NO:144) CTCTGATGTGAGGGG; (SEQ ID NO:145) CCTGGCCCCCCACTC; (SEQ ID NO:146) CTCTGATGTGAGGAG; (SEQ ID NO:147) GAACCCTCCCTCCGC; (SEQ ID NO:148) GCTGGCTGCGATGCG; (SEQ ID NO:149) GAACCCTCCCTCCAC; (SEQ ID NO:150) GCTGGCTGCGATGTG; (SEQ ID NO:151) TAGATACACCTGCTG; (SEQ ID NO:152) GCAGATACACCACAG; (SEQ ID NO:153) TAGATACACCTGCCG; (SEQ ID NO:154) GCAGATACACCACGG; (SEQ ID NO:155) GAAGGCATGTCTGAA; (SEQ ID NO:156) ATGGCTGTCTACTTC; (SEQ ID NO:157) GAAGGCATGTCTGCA; (SEQ ID NO:158) ATGGCTGTCTACTGC; (SEQ ID NO:159) GAACCCTGACCAACC; (SEQ ID NO:160) TGCAAAAGCAAAGGA; (SEQ ID NO:161) GAACCCTGACCAATC; (SEQ ID NO:162) TGCAAAAGCAAAGAA; (SEQ ID NO:163) TCTTGCCCTGTTTTC; (SEQ ID NO:164) TGTTGTGCTCCAGAA; (SEQ ID NO:165) TCTTGCCCTGTTTCC; (SEQ ID NO:166) TGTTGTGCTCCAGGA; (SEQ ID NO:167) TGTTCCTGGACCTGC; (SEQ ID NO:168) TCTCCTCTCCGAGCA; (SEQ ID NO:169) TGTTCCTGGACCTTC; (SEQ ID NO:170) TCTOCTCTCCGAGAA; (SEQ ID NO:171) TGGGGGAGTCATGCC; (SEQ ID NO:172) AAGGTGGAAGAAGGC; (SEQ ID NO:173) TGGGGGAGTCATGTC; (SEQ ID NQ:174) AAGGTGGAAGAAGAC; (SEQ ID NO:175) AGTCATGCCTTCTTC; (SEQ ID NO:176) TTCCCGAAGGTGGAA; (SEQ ID NO:177) AGTCATGCCTTCTCC; (SEQ ID NO:178) TTCCCGAAGGTGGGA; (SEQ ID NO:179) CAGCTGCAGCCCCCG; (SEQ ID NO:180) TGGGGGCCGAGACGG; (SEQ ID NO:181) CAGCTGCAGCCCCTG; (SEQ ID NO:182) TGGGGGCCGAGACAG; (SEQ ID NO:183) CTATCAGGAGTTTGT; (SEQ ID NO:184) TCCACCGCATGTACA; (SEQ ID NQ:135) CTATCAGGAGTTTAT; (SEQ ID NO:186) TCCACCGCATGTATA; (SEQ ID NO:187) CCCAAGCAGCTCCCC; (SEQ ID NO:188) CCCAGGTGCTCTGGG; (SEQ ID NO:189) CCCAAGCAGCTCCTC; (SEQ ID NO:190) CCCAGGTGCTCTGAG; (SEQ ID NO:191) CTGTGGAGACAGGTC; (SEQ ID NO:192) GTAGGGGGCGAGGAC; (SEQ ID NO:193) CTGTGGAGACAGGGC; (SEQ ID NO:194) GTAGGGGGCGAGGCC; (SEQ ID NO:195) TCCATCCTGCCCCTG; (SEQ ID NO:196) TCTGAGCATTGCCAG; (SEQ ID NO:197) TCCATCCTGCCCCCG; (SEQ ID NO:198) TCTGAGCATTGCCGG; (SEQ ID NO:199) TCTCTTAGGTGCATG; (SEQ ID NO:200) GCAACAAGAGGACAT; (SEQ ID NO:201) TCTCTTAGGTGCACG; (SEQ ID NO:202) GCAACAAGAGGACGT; (SEQ ID NO:203) TCTTAGGTGCATGTC; (SEQ ID NO:204) CAGCAACAAGAGGAC; (SEQ ID NO:205) TCTTAGGTGCATGCC; (SEQ ID NO:206) CAGCAACAAGAGGGC; (SEQ ID NO:207) GACTAGGGCTTATCC; (SEQ ID NO:208) TTTCCCAGGCATGGA; (SEQ ID NO:209) GACTAGGGCTTATTC; (SEQ ID NO:210) TTTCCCAGGCATGAA; (SEQ ID NO:211) GAAGGCAGCCAGGCT; (SEQ ID NO:212) TGGAAATCTGCCAGC; (SEQ ID NO:213) GAAGGCAGCCAGGGT; (SEQ ID NO:214) TGGAAATCTGCCACC; (SEQ ID NO:215) GATCATGGCCCACAT; (SEQ ID NO:216) AGGTGGGCCTCCATG; (SEQ ID NO:217) GATCATGGCCCACGT; (SEQ ID NO:213) AGGTGGGCCTCCACG; (SEQ ID NO:219) AGAAACTAACACAGC; (SEQ ID NO:220) ATTCCCTTGATGGCT; (SEQ ID NO:221) AGAAACTAACACAAC; (SEQ ID NO:222) ATTCCCTTGATGGTT; (SEQ ID NO:223) GTTGAGTAATGCTCG; (SEQ ID NO:224) AAAACACACAGACGA; (SEQ ID NO:225) GTTGAGTAATGCTTG; (SEQ ID NO:226) AAAACACACAGACAA; (SEQ ID NO:227) TAAGAAACTTGCCGT; (SEQ ID NO:228) ACCCAAACCCAGACG; (SEQ ID NO:229) TAAGAAACTTGCCAT; (SEQ ID NO:230) and ACCCAAACCCAGATG. (SEQ ID NO:231)

[0104] Other genotyping oligonucleotides of the invention hybridize to a target region located one to several nucleotides downstream of one of the novel polymorphic sites identified herein. Such oligonucleotides are useful in polymerase-mediated primer extension methods for detecting one of the novel polymorphisms described herein and therefore such genotyping oligonucleotides are referred to herein as “primer-extension oligonucleotides”. In a preferred embodiment, the 3′-terminus of a primer-extension oligonucleotide is a deoxynucleotide complementary to the nucleotide located immediately adjacent to the polymorphic site. A particularly preferred oligonucleotide primer for detecting IL4Rα gene polymorphisms by primer extension terminates in a nucleotide sequence, listed 5′ to 3′, selected from the group consisting of: AGATTGCACC; (SEQ ID NO:232) TGGAGTGCAG; (SEQ ID NO:233) TGCTTTTGTG; (SEQ ID NO:234) AAGGGGAATA; (SEQ ID NO:235) TTCCTGGGCC; (SEQ ID NO:236) GCAGCCTGAG; (SEQ ID NO:237) GAGTAAGCCT; (SEQ ID NO:238) AGCTCCAGCG; (SEQ ID NO:239) CTGAGAACAA; (SEQ ID NO:240) CCGCGCCTCC; (SEQ ID NO:241) CAACGGAGGC; (SEQ ID NO:242) ACGCACCCCG; (SEQ ID NO:243) TCAGTGCGGA; (SEQ ID NO:244) GTGTATAGTT; (SEQ ID NO:245) GGGCGGAGTG; (SEQ ID NO:246) CACCCCTGCC; (SEQ ID NO:247) GCTGCCTGGG; (SEQ ID NO:248) CCCACCCTCA; (SEQ ID NO:249) GGGTGGGGTG; (SEQ ID NO:250) CCTCCCCTGC; (SEQ ID NO:251) CGCTTCTCCC; (SEQ ID NO:252) GGTTTCACTG; (SEQ ID NO:253) GGAGTGGAAA; (SEQ ID NO:254) CTGCCGGGTC; (SEQ ID NO:255) GGAGGCAAGC; (SEQ ID NO:256) CCAGCCCCAG; (SEQ ID NO:257) CAAGCCCTGG; (SEQ ID NO:258) GCTATCCAGC; (SEQ ID NO:259) TGGATAGCAA; (SEQ ID NO:260) GCTCCTGGGA; (SEQ ID NO:261) CTGGCTCTGC; (SEQ ID NO:262) ACTTGCCTAG; (SEQ ID NO:263) GGCCCCCCAC; (SEQ ID NO:264) TGATGTGAGG; (SEQ ID NO:265) CCCTCCCTCC; (SEQ ID NO:266) GGCTGCGATG; (SEQ ID NO:267) ATACACCTGC; (SEQ ID NO:268) GATACACCAC; (SEQ ID NO:269) GGCATGTCTG; (SEQ ID NO:270) GCTGTCTACT; (SEQ ID NO:271) CCCTGACCAA; (SEQ ID NO:272) AAAAGCAAAG; (SEQ ID NO:273) TGCCCTGTTT; (SEQ ID NO:274) TGTGCTCCAG; (SEQ ID NO:275) TCCTGGACCT; (SEQ ID NO:276) CCTCTCCGAG; (SEQ ID NO:277) GGGAGTCATG; (SEQ ID NO:278) GTGGAAGAAG; (SEQ ID NO:279) CATGCCTTCT; (SEQ ID NQ:280) CCGAAGGTGG; (SEQ ID NO:281) CTGCAGCCCC; (SEQ ID NO:232) GGGCCGAGAC; (SEQ ID NQ:283) TCAGGAGTTT; (SEQ ID NO:284) ACCGCATGTA; (SEQ ID NO:285) AAGCAGCTCC; (SEQ ID NO:286) AGGTGCTCTG; (SEQ ID NO:287) TGGAGACAGG; (SEQ ID NO:288) GGGGGCGAGG; (SEQ ID NO:289) ATCCTGCCCC; (SEQ ID NO:290) GAGCATTGCO; (SEQ ID NO:291) CTTAGGTGCA; (SEQ ID NO:292) ACAAGAGGAC; (SEQ ID NO:293) TAGGTGCATG; (SEQ ID NO:294) CAACAAGAGG; (SEQ ID NO:295) TAGGGCTTAT; (SEQ ID NO:296) CCCAGGCATG; (SEQ ID NO:297) GGCAGCCAGG; (SEQ ID NO:298) AAATCTGCCA; (SEQ ID NO:299) CATGGCCCAC; (SEQ ID N0:300) TGGGCCTCCA; (SEQ ID NO:301) AACTAACACA; (SEQ ID NO:302) COCTTGATGG; (SEQ ID NO:303) GAGTAATGCT; (SEQ ID NO:304) ACACACAGAC; (SEQ ID NO:305) GAAACTTGCC; (SEQ ID NO:306) and CAAACCCAGA. (SEQ ID NO:307)

[0105] In some embodiments, a composition contains two or more differently labeled genotyping oligonucleotides for simultaneously probing the identity of nucleotides at two or more polymorphic sites. It is also contemplated that primer compositions may contain two or more sets of allele-specific primer pairs to allow simultaneous targeting and amplification of two or more regions containing a polymorphic site.

[0106] IL4Rα genotyping oligonucleotides of the invention may also be immobilized on or synthesized on a solid surface such as a microchip, bead, or glass slide (see, e.g., WO 98/20020 and WO 98/20019). Such immobilized genotyping oligonucleotides may be used in a variety of polymorphism detection assays, including but not limited to probe hybridization and polymerase extension assays. Immobilized IL4Rα genotyping oligonucleotides of the invention may comprise an ordered array of oligonucleotides designed to rapidly screen a DNA sample for polymorphisms in multiple genes at the same time.

[0107] In another embodiment, the invention provides a kit comprising at least two genotyping oligonucleotides packaged in separate containers. The kit may also contain other components such as hybridization buffer (where the oligonucleotides are to be used as a probe) packaged in a separate container. Alternatively, where the oligonucleotides are to be used to amplify a target region, the kit may contain, packaged in separate containers, a polymerase and a reaction buffer optimized for primer extension mediated by the polymerase, such as PCR.

[0108] The above described oligonucleotide compositions and kits are useful in methods for genotyping and/or haplotyping the IL4Rα gene in an individual. As used herein, the terms “IL4Rα genotype” and “IL4Rα haplotype” mean the genotype or haplotype contains the nucleotide pair or nucleotide, respectively, that is present at one or more of the novel polymorphic sites described herein and may optionally also include the nucleotide pair or nucleotide present at one or more additional polymorphic sites in the IL4Rα gene. The additional polymorphic sites may be currently known polymorphic sites or sites that are subsequently discovered.

[0109] One embodiment of the genotyping method involves isolating from the individual a nucleic acid mixture comprising the two copies of the IL4Rα gene, or a fragment thereof, that are present in the individual, and determining the identity of the nucleotide pair at one or more of the polymorphic sites selected from PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45 in the two copies to assign an IL4Rα genotype to the individual. As will be readily understood by the skilled artisan, the tow “copies” of a gene in an individual may be the same allele or may be different alleles. In a preferred embodiment of the genotyping method, the identity of the nucleotide pair atone or more of the polymorphic sites selected from the group consisting of PS5, PS24, PS26, PS29, PS31, PS42, and PS43 is also determined. In a particularly preferred embodiment, the genotyping method comprises determining the identity of the nucleotide pair at each of PS1-45.

[0110] Typically, the nucleic acid mixture is isolated from a biological sample taken from the individual, such as a blood sample or tissue sample. Suitable tissue samples include whole blood, semen saliva, tears, urine, fecal material, sweat, buccal, skin and hair. The nucleic acid mixture may be comprised of genomic DNA, mRNA, or cDNA and, in the latter two cases, the biological sample must be obtained from an organ in which the IL4Rα gene is expressed. Furthermore it will be understood by the skilled artisan that mRNA or cDNA preparations would not be used to detect polymorphisms located in introns or in 5′ and 3′ nontranscribed regions. If an IL4Rα gene fragment is isolated, it must contain the polymorphic site(s) to be genotyped.

[0111] One embodiment of the haplotyping method comprises isolating from the individual a nucleic acid molecule containing only one of the two copies of the IL4Rα gene, or a fragment thereof, that is present in the individual and determining in that copy the identity of the nucleotide at one or more of the polymorphic sites PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45 in that copy to assign an IL4Rα haplotype to the individual. The nucleic acid may be isolated using any method capable of separating the two copies of the IL4Rα gene or fragment such as one of the methods described above for preparing IL4Rα isogenes, with targeted in vivo cloning being the preferred approach. As will be readily appreciated by those skilled in the art, any individual clone will only provide haplotype information on one of the two IL4Rα gene copies present in an individual. If haplotype information is desired for the individual's other copy, additional IL4Rα clones will need to be examined. Typically, at least five clones should be examined to have more than a 90% probability of haplotyping both copies of the IL4Rα gene in an individual. In some embodiments, the haplotyping method also comprises identifying the nucleotide atone or more of the polymorphic sites PS5, PS24, PS26, PS29, PS31, PS42, and PS43. In a particularly preferred embodiment, the nucleotide at each of PS1-45 is identified.

[0112] In a preferred embodiment, an IL4Rα haplotype pair is determined for an individual by identifying the phased sequence of nucleotides at one or more of the polymorphic sites selected from PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45 in each copy of the IL4Rα gene that is present in the individual. In a particularly preferred embodiment, the haplotyping method comprises identifying the phased sequence of nucleotides at each of PS1-45 in each copy of the IL4Rα gene. When haplotyping both copies of the gene, the identifying step is preferably performed with each copy of the gene being placed in separate containers. However, it is also envisioned that if the two copies are labeled with different tags, or are otherwise separately distinguishable or identifiable, it could be possible in some cases to perform the method in the same container. For example, if first and second copies of the gene are labeled with different first and second fluorescent dyes, respectively, and an allele-specific oligonucleotide labeled with yet a third different fluorescent dye is used to assay the polymorphic site(s), then detecting a combination of the first and third dyes would identify the polymorphism in the first gene copy while detecting a combination of the second and third dyes would identify the polymorphism in the second gene copy.

[0113] In both the genotyping and haplotyping methods, the identity of a nucleotide (or nucleotide pair) at a polymorphic site(s) may be determined by amplifying a target region(s) containing the polymorphic site(s) directly from one or both copies of the IL4Rα gene, or fragment thereof, and the sequence of the amplified region(s) determined by conventional methods. It will be readily appreciated by the skilled artisan that only one nucleotide will be detected at a polymorphic site in individuals who are homozygous at that site, while two different nucleotides will be detected if the individual is heterozygous for that site. The polymorphism may be identified directly, known as positive-type identification, or by inference, referred to as negative-type identification. For example, where a SNP is known to be guanine and cytosine in a reference population, a site may be positively determined to be either guanine or cytosine for an individual homozygous at that site, or both guanine and cytosine, if the individual is heterozygous at that site. Alternatively, the site may be negatively determined to be not guanine (and thus cytosine/cytosine) or not cytosine (and thus guanine/guanine).

[0114] In addition, the identity of the allele(s) present at any of the novel polymorphic sites described herein may be indirectly determined by genotyping a polymorphic site not disclosed herein that is in linkage disequilibrium with the polymorphic site that is of interest. Two sites are said to be in linkage disequilibrium if the presence of a particular variant at one site enhances the predictability of another variant at the second site (Stevens, JC 1999, Mol. Diag. 4: 309-17). Polymorphic sites in linkage disequilibrium with the presently disclosed polymorphic sites may be located in regions of the gene or in other genomic regions not examined herein. Genotyping of a polymorphic site in linkage disequilibrium with the novel polymorphic sites described herein may be performed by, but is not limited to, any of the above-mentioned methods for detecting the identity of the allele at a polymorphic site.

[0115] The target region(s) may be amplified using any oligonucleotide-directed amplification method, including but not limited to polymerase chain reaction (PCR) (U.S. Pat. No. 4,965,188), ligase chain reaction (LCR) (Barany et al., Proc. Natl. Acad. Sci. USA 88:189-193, 1991; WO90/01069), and oligonucleotide ligation assay (OLA) (Landegren et al., Science 241:1077-1080, 1988). Oligonucleotides useful as primers or probes in such methods should specifically hybridize to a region of the nucleic acid that contains or is adjacent to the polymorphic site. Typically, the oligonucleotides are between 10 and 35 nucleotides in length and preferably, between 15 and 30 nucleotides in length. Most preferably, the oligonucleotides are 20 to 25 nucleotides long. The exact length of the oligonucleotide will depend on many factors that are routinely considered and practiced by the skilled artisan.

[0116] Other known nucleic acid amplification procedures may be used to amplify the target region including transcription-based amplification systems (U.S. Pat. No. 5,130,238; EP 329,822; U.S. Pat. No. 5,169,766, WO89/06700) and isothermal methods (Walker et al., Proc. Natl. Acad. Sci. USA 89:392-396, 1992).

[0117] A polymorphism in the target region may also be assayed before or after amplification using one of several hybridization-based methods known in the art. Typically, allele-specific oligonucleotides are utilized in performing such methods. The allele-specific oligonucleotides may be used as differently labeled probe pairs, with one member of the pair showing a perfect match to one variant of a target sequence and the other member showing a perfect match to a different variant. In some embodiments, more than one polymorphic site may be detected at once using a set of allele-specific oligonucleotides or oligonucleotide pairs. Preferably, the members of the set have melting temperatures within 5° C., and more preferably within 2° C., of each other when hybridizing to each of the polymorphic sites being detected.

[0118] Hybridization of an allele-specific oligonucleotide to a target polynucleotide may be performed with both entities in solution, or such hybridization may be performed when either the oligonucleotide or the target polynucleotide is covalently or noncovalently affixed to a solid support. Attachment may be mediated, for example, by antibody-antigen interactions, poly-L-Lys, streptavidin or avidin-biotin, salt bridges, hydrophobic interactions, chemical linkages, UV cross-linking baking, etc. Allele-specific oligonucleotides may be synthesized directly on the solid support or attached to the solid support subsequent to synthesis. Solid-supports suitable for use in detection methods of the invention include substrates made of silicon, glass, plastic, paper and the like, which may be formed, for example, into wells (as in 96-well plates), slides, sheets, membranes, fibers, chips, dishes, and beads. The solid support may be treated, coated or derivatized to facilitate the immobilization of the allele-specific oligonucleotide or target nucleic acid.

[0119] The genotype or haplotype for the IL4Rα gene of an individual may also be determined by hybridization of a nucleic sample containing one or both copies of the gene to nucleic acid arrays and subarrays such as described in WO 95/11995. The arrays would contain a battery of allele-specific oligonucleotides representing each of the polymorphic sites to be included in the genotype or haplotype.

[0120] The identity of polymorphisms may also be determined using a mismatch detection technique, including but not limited to the RNase protection method using riboprobes (Winter et al., Proc. Natl. Acad. Sci. USA 82:7575, 1985; Meyers et al., Science 230:1242, 1985) and proteins which recognize nucleotide mismatches, such as the E. coli mutS protein (Modrich, P. Ann. Rev. Genet. 25:229-253, 1991). Alternatively, variant alleles can be identified by single strand conformation polymorphism (SSCP) analysis (Orita et al., Genomics 5:874-879, 1989; Humphries et al., in Molecular Diagnosis of Genetic Diseases, R. Elles, ed., pp. 321-340, 1996) or denaturing gradient gel electrophoresis (DGGE) (Wartell et al., Nucl. Acids Res. 18:2699-2706, 1990; Sheffield et al., Proc. Natl. Acad. Sci. USA 86:232-236, 1989).

[0121] A polymerase-mediated primer extension method may also be used to identify the polymorphism(s). Several such methods have been described in the patent and scientific literature and include the “Genetic Bit Analysis” method (WO92/15712) and the ligase/polymerase mediated genetic bit analysis (U.S. Pat. No. 5,679,524. Related methods are disclosed in WO91/02087, WO90/09455, WO95/17676, U.S. Pat. Nos. 5,302,509, and 5,945,283. Extended primers containing a polymorphism may be detected by mass spectrometry as described in U.S. Pat. No. 5,605,798. Another primer extension method is allele-specific PCR (Ruaño et al., Nucl. Acids Res. 17:8392, 1989; Ruaño et al., Nucl. Acids Res. 19, 6877-6882, 1991; WO 93/22456; Turki et al., J. Clin. Invest. 95:1635-1641, 1995). In addition, multiple polymorphic sites may be investigated by simultaneously amplifying multiple regions of the nucleic acid using sets of allele-specific primers as described in Wallace et al. (WO89/10414).

[0122] In another aspect of the invention, an individual's IL4Rα haplotype pair is predicted from its IL4Rα genotype using information on haplotype pairs known to exist in a reference population. In its broadest embodiment, the haplotyping prediction method comprises identifying an IL4Rα genotype for the individual at two or more polymorphic sites selected from PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, PS45, enumerating all possible haplotype pairs which are consistent with the genotype, accessing data containing IL4Rα haplotype pairs identified in a reference population, and assigning a haplotype pair to the individual that is consistent with the data. In one embodiment, the reference haplotype pairs include the IL4Rα haplotype pairs shown in Table 4.

[0123] Generally, the reference population should be composed of randomly-selected individuals representing the major ethnogeographic groups of the world. A preferred reference population for use in the methods of the present invention comprises an approximately equal number of individuals from Caucasian, African American, Asian and Hispanic-Latino population groups with the minimum number of each group being chosen based on how rare a haplotype one wants to be guaranteed to see. For example, if one wants to have a q% chance of not missing a haplotype that exists in the population at a p% frequency of occurring in the reference population, the number of individuals (n) who must be sampled is given by 2n=log(1-q)/log(1-p) where p and q are expressed as fractions. A preferred reference population allows the detection of any haplotype whose frequency is at least 10% with about 99% certainty and comprises about 20 unrelated individuals from each of the four population groups named above. A particularly preferred reference population includes a 3-generation family representing one or more of the four population groups to serve as controls for checking quality of haplotyping procedures.

[0124] In a preferred embodiment, the haplotype frequency data for each ethnogeographic group is examined to determine whether it is consistent with Hardy-Weinberg equilibrium. Hardy-Weinberg equilibrium (D. L. Hartl et al., Principles of Population Genomics, Sinauer Associates (Sunderland, Mass.), 3^(rd) Ed., 1997) postulates that the frequency of finding the haplotype pair H₁/H₂ is equal to p_(H−W) (H₁/H₂)=2p(H₁)p(H₂) if H₁≠H₂ and p_(H−W)(H₁/H₂)=p(H₁)p(H₂) if H₁=H₂. A statistically significant difference between the observed and expected haplotype frequencies could be due to one or more factors including significant inbreeding in the population group, strong selective pressure on the gene, sampling bias, and/or errors in the genotyping process. If large deviations from Hardy-Weinberg equilibrium are observed in an ethnogeographic group, the number of individuals in that group can be increased to see if the deviation is due to a sampling bias. If a larger sample size does not reduce the difference between observed and expected haplotype pair frequencies, then one may wish to consider haplotyping the individual using a direct haplotyping method such as, for example, CLASPER System™ technology (U.S. Pat. No. 5,866,404), SMD, or allele-specific long-range PCR (Michalotos-Beloin et al., Nucleic Acids Res. 24:4841-4843, 1996).

[0125] In one embodiment of this method for predicting an IL4Rα haplotype pair, the assigning step involves performing the following analysis. First, each of the possible haplotype pairs is compared to the haplotype pairs in the reference population. Generally, only one of the haplotype pairs in the reference population matches a possible haplotype pair and that pair is assigned to the individual. Occasionally, only one haplotype represented in the reference haplotype pairs is consistent with a possible haplotype pair for an individual, and in such cases the individual is assigned a haplotype pair containing this known haplotype and a new haplotype derived by subtracting the known haplotype from the possible haplotype pair. In rare cases, either no haplotypes in the reference population are consistent with the possible haplotype pairs, or alternatively, multiple reference haplotype pairs are consistent with the possible haplotype pairs. In such cases, the individual is preferably haplotyped using a direct molecular haplotyping method such as, for example, CLASPER System™ technology (U.S. Pat. No. 5,866,404), SMD, or allele-specific long-range PCR (Michalotos-Beloin et al., Nucleic Acids Res. 24:4841-4843, 1996).

[0126] The invention also provides a method for determining the frequency of an IL4Rα genotype or IL4Rα haplotype in a population. The method comprises determining the genotype or the haplotype pair for the IL4Rα gene that is present in each member of the population, wherein the genotype or haplotype comprises the nucleotide pair or nucleotide detected at one or more of the polymorphic sites PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45 in the IL4Rα gene; and calculating the frequency any particular genotype or haplotype is found in the population. The population may be a reference population, a family population, a same sex population, a population group, a trait population (e.g., a group of individuals exhibiting a trait of interest such as a medical condition or response to a therapeutic treatment).

[0127] In another aspect of the invention, frequency data for IL4Rα genotypes and/or haplotypes found in a reference population are used in a method for identifying an association between a trait and an IL4Rα genotype or an IL4Rα haplotype. The trait may be any detectable phenotype, including but not limited to susceptibility to a disease or response to a treatment. The method involves obtaining data on the frequency of the genotype(s) or haplotype(s) of interest in a reference population as well as in a population exhibiting the trait. Frequency data for one or both of the reference and trait populations may be obtained by genotyping or haplotyping each individual in the populations using one of the methods described above. The haplotypes for the trait population may be determined directly or, alternatively, by the predictive genotype to haplotype approach described above. In another embodiment, the frequency data for the reference and/or trait populations is obtained by accessing previously determined frequency data, which may be in written or electronic form. For example, the frequency data may be present in a database that is accessible by a computer. Once the frequency data is obtained, the frequencies of the genotype(s) or haplotype(s) of interest in the reference and trait populations are compared. In a preferred embodiment, the frequencies of all genotypes and/or haplotypes observed in the populations are compared. If a particular genotype or haplotype for the IL4Rα gene is more frequent in the trait population than in the reference population at a statistically significant amount, then the trait is predicted to be associated with that IL4Rα genotype or haplotype. Preferably, the IL4Rα genotype or haplotype being compared in the trait and reference populations is selected from the full-genotypes and full-haplotypes shown in Tables 4 and 5, respectively, or from sub-genotypes and sub-haplotypes derived from these genotypes and haplotypes.

[0128] In a preferred embodiment of the method, the trait of interest is a clinical response exhibited by a patient to some therapeutic treatment, for example, response to a drug targeting IL4Rα or response to a therapeutic treatment for a medical condition. As used herein, “medical condition” includes but is not limited to any condition or disease manifested as one or more physical and/or psychological symptoms for which treatment is desirable, and includes previously and newly identified diseases and other disorders. As used herein the term “clinical response” means any or all of the following: a quantitative measure of the response, no response, and adverse response (i.e., side effects).

[0129] In order to deduce a correlation between clinical response to a treatment and an IL4Rα genotype or haplotype, it is necessary to obtain data on the clinical responses exhibited by a population of individuals who received the treatment, hereinafter the “clinical population”. This clinical data may be obtained by analyzing the results of a clinical trial that has already been run and/or the clinical data may be obtained by designing and carrying out one or more new clinical trials. As used herein, the term “clinical trial” means any research study designed to collect clinical data on responses to a particular treatment, and includes but is not limited to phase I, phase II and phase III clinical trials. Standard methods are used to define the patient population and to enroll subjects.

[0130] It is preferred that the individuals included in the clinical population have been graded for the existence of the medical condition of interest. This is important in cases where the symptom(s) being presented by the patients can be caused by more than one underlying condition, and where treatment of the underlying conditions are not the same. An example of this would be where patients experience breathing difficulties that are due to either asthma or respiratory infections. If both sets were treated with an asthma medication, there would be a spurious group of apparent non-responders that did not actually have asthma. These people would affect the ability to detect any correlation between haplotype and treatment outcome. This grading of potential patients could employ a standard physical exam or one or more lab tests. Alternatively, grading of patients could use haplotyping for situations where there is a strong correlation between haplotype pair and disease susceptibility or severity.

[0131] The therapeutic treatment of interest is administered to each individual in the trial population and each individual's response to the treatment is measured using one or more predetermined criteria. It is contemplated that in many cases, the trial population will exhibit a range of responses and that the investigator will choose the number of responder groups (e.g., low, medium, high) made up by the various responses. In addition, the IL4Rα gene for each individual in the trial population is genotyped and/or haplotyped, which may be done before or after administering the treatment.

[0132] After both the clinical and polymorphism data have been obtained, correlations between individual response and IL4Rα genotype or haplotype content are created. Correlations may be produced in several ways. In one method, individuals are grouped by their IL4Rα genotype or haplotype (or haplotype pair) (also referred to as a polymorphism group), and then the averages and standard deviations of clinical responses exhibited by the members of each polymorphism group are calculated.

[0133] These results are then analyzed to determine if any observed variation in clinical response between polymorphism groups is statistically significant. Statistical analysis methods which may be used are described in L. D. Fisher and G. vanBelle, “Biostatistics: A Methodology for the Health Sciences”, Wiley-Interscience (New York) 1993. This analysis may also include a regression calculation of which polymorphic sites in the IL4Rα gene give the most significant contribution to the differences in phenotype. One regression model useful in the invention starts with a model of the form

r=r ₀ +S×d

[0134] where r is the response, r₀ is a constant called the “intercept”, S is the slope and d is the dose. To determine the dose, the most-common and least common nucleotides at the polymorphic site are first defined. Then, for each individual in the trial population, one calculates a “dose” as the number of least-common nucleotides the individual has at the polymorphic site of interest. This value can be 0 (homozygous for the least-common nucleotide), 1 (heterozygous), or 2 (homozygous for the most common nucleotide). An individual's “response” is the value of the clinical measurement. Standard linear regression methods are then used to fit all the individuals' doses and responses to a single model (see e.g., L. D. Fisher and G. vanBelle, supra, Ch 9). The outputs of the regression calculation are the intercept r₀, the slope S, and the variance (which measures how well the data fits this simple linear model). The Students t-test value and the level of significance can then be calculated for each of the polymorphic sites.

[0135] A second method for finding correlations between IL4Rα haplotype content and clinical responses uses predictive models based on error-minimizing optimization algorithms. One of many possible optimization algorithms is a genetic algorithm (R. Judson, “Genetic Algorithms and Their Uses in Chemistry” in Reviews in Computational Chemistry, Vol. 10, pp. 1-73, K. B. Lipkowitz and D. B. Boyd, eds. (VCH Publishers, New York, 1997). Simulated annealing (Press et al., “Numerical Recipes in C: The Art of Scientific Computing”, Cambridge University Press (Cambridge) 1992, Ch. 10), neural networks (E. Rich and K. Knight, “Artificial Intelligence”, 2^(nd) Edition (McGraw-Hill, New York, 1991, Ch. 18), standard gradient descent methods (Press et al., supra Ch. 10), or other global or local optimization approaches (see discussion in Judson, supra) could also be used. As an example, a genetic algorithm approach is described herein. This method searches for optimal parameters or weights in linear or Don-linear models connecting IL4Rα haplotype loci and clinical outcome. One model is of the form $\begin{matrix} {C = {C_{0} + {\sum\limits_{\alpha}\left( {{\sum\limits_{t}{w_{i,\alpha}R_{i,\alpha}}} + {\sum\limits_{i}{w_{i,\alpha}^{\prime}L_{i,\alpha}}}} \right)}}} & \lbrack 1\rbrack \end{matrix}$

[0136] where C is the measured clinical outcome, i goes over all polymorphic sites, α over all candidate genes, C₀, w_(i,α)and w′_(i,α) are variable weight values, R_(i,α) is equal to 1 if site i in gene α in the first haplotype takes on the most common nucleotide and −1 if it takes on the less common nucleotide. L_(i,α) is the same as R_(i,α) except for the second haplotype. The constant term C₀ and the weights w_(i,α) and w′_(i,α) are varied by the genetic algorithm during a search process that minimizes the error between the measured value of C and the value calculated from Equation 1. Models other than the one given in Equation 1 can be readily incorporated by those skilled in the art for analyzing the clinical and polymorphism data. The genetic algorithm is especially suited for searching not only over the space of weights in a particular model but also over the space of possible models (Judson, supra).

[0137] Correlations may also be analyzed using analysis of variation (ANOVA) techniques to determine how much of the variation in the clinical data is explained by different subsets of the polymorphic sites in the IL4Rα gene. ANOVA is used to test hypotheses about whether a response variable is caused by or correlated with one or more traits or variables that can be measured (Fisher and vanBelle, supra, Ch. 10). These traits or variables are called the independent variables. To carry out ANOVA, the independent variable(s) are measured and individuals are placed into groups based on their values for these variables. In this case, the independent variable(s) refers to the combination of polymorphisms present at a subset of the polymorphic sites, and thus, each group contains those individuals with a given genotype or haplotype pair. The variation in response within the groups and also the variation between groups is then measured. If the within-group response variation is large (people in a group have a wide range of responses) and the response variation between groups is small (the average responses for all groups are about the same) then it can be concluded that the independent variables used for the grouping are not causing or correlated with the response variable. For instance, if people are grouped by month of birth (which should have nothing to do with their response to a drug) the ANOVA calculation should show a low level of significance. However, if the response variation is larger between groups than within groups, the F-ratio (=“between groups” divided by “within groups”) is greater than one. Large values of the F-ratio indicate that the independent variable is causing or correlated with the response. The calculated F-ratio is preferably compared with the critical F-distribution value at whatever level of significance is of interest. If the F-ratio is greater than the Critical F-distribution value, then one may be confident that the individual's genotype or haplotype pair for this particular subset of polymorphic sites in the IL4Rα gene is at least partially responsible for, or is at least strongly correlated with the clinical response.

[0138] From the analyses described above, a mathematical model may be readily constructed by the skilled artisan that predicts clinical response as a function of IL4Rα genotype or haplotype content. Preferably, the model is validated in one or more follow-up clinical trials designed to test the model.

[0139] The identification of an association between a clinical response and a genotype or haplotype (or haplotype pair) for the IL4Rα gene may be the basis for designing a diagnostic method to determine those individuals who will or will not respond to the treatment, or alternatively, will respond at a lower level and thus may require more treatment, i.e., a greater dose of a drug. The diagnostic method may take one of several forms: for example, a direct DNA test (i.e., genotyping or haplotyping one or more of the polymorphic sites in the IL4Rα gene), a serological test, or a physical exam measurement. The only requirement is that there be a good correlation between the diagnostic test results and the underlying IL4Rα genotype or haplotype that is in turn correlated with the clinical response. In a preferred embodiment, this diagnostic method uses the predictive haplotyping method described above.

[0140] Any or all analytical and mathematical operations involved in practicing the methods of the present invention may be implemented by a computer. In addition, the computer may execute a program that generates views (or screens) displayed on a display device and with which the user can interact to view and analyze large amounts of information relating to the IL4Rα gene and its genomic variation, including chromosome location, gene structure, and gene family, gene expression data, polymorphism data, genetic sequence data, and clinical data population data (e.g., data on ethnogeographic origin, clinical responses, genotypes, and haplotypes for one or more populations). The IL4Rα polymorphism data described herein may be stored as part of a relational database (e.g., an instance of an Oracle database or a set of ASCII flat files). These polymorphism data may be stored on the computer's hard drive or may, for example, be stored on a CD ROM or on one or more other storage devices accessible by the computer. For example, the data may be stored on one or more databases in communication with the computer via a network.

[0141] Preferred embodiments of the invention are described in the following examples. Other embodiments within the scope of the claims herein will be apparent to one skilled in the art from consideration of the specification or practice of the invention as disclosed herein. It is intended that the specification, together with the examples, be considered exemplary only, with the scope and spirit of the invention being indicated by the claims which follow the examples.

EXAMPLES

[0142] The Examples herein are meant to exemplify the various aspects of carrying out the invention and are not intended to limit the scope of the invention in any way. The Examples do not include detailed descriptions for conventional methods employed, such as in the performance of genomic DNA isolation, PCR and sequencing procedures. Such methods are well-known to those skilled in the art and are described in numerous publications, for example, Sambrook, Fritsch, and Maniatis, “Molecular Cloning: A Laboratory Manual”, ₂nd Edition, Cold Spring Harbor Laboratory Press, USA, (1989).

Example 1A

[0143] This example illustrates examination of various regions of the IL4Rα gene for polymorphic sites using DNA from Index Repository IA.

[0144] Amplification of Target Regions

[0145] The following target regions of the IL4Rα gene were amplified using the PCR primer pairs listed below, with the sequences presented in the 5′ to 3′ direction and nucleotide positions shown for each region corresponding to the indicated GenBank Accession No. Accession Number: AC004525 Fragment 1 Forward Primer 32801-32822 CCACAGTCATCCCGACACTAGC (SEQ ID NO:308) Reverse Primer Complement of 33355-33334 TATTCCAGCCGTATCCATGTGC (SEQ ID NO: 309) PCR product 555 nt Fragment 2 Forward Primer 35515-35536 CCTTGGTGCATGTGGTAAGAGG (SEQ ID NO:310) Reverse Primer Complement of 36068-36046 TTTCAAAGGTGGGAGGACTGAGG (SEQ ID NO:311) PCR product 554 nt Fragment 3 Forward Primer 37031-37050 GCAGTGAGCTGGGATTGTGC (SEQ ID NO:312) Reverse Primer Complement of 37701-37679 AACTCCCCTTCTCTGATGTGAGG (SEQ ID NO:313) PCR product 671 nt Fragment 4 Forward Primer 43240-43262 TCACAGTTACAGAGGTGGCAAGC (SEQ ID NO:314) Reverse Primer Complement of 43727-43706 CTGCCTACCTGGCAGATACACC (SEQ ID NO:315) PCR product 488 nt Fragment 5 Forward Primer 49553-49574 AGCTGTCACTCCACCTCCTTGG (SEQ ID NO:316) Reverse Primer Complement of 50036-50013 AAAGCCTCTGGTCTGCTAATGACC (SEQ ID NO:317) PCR product 484 nt Fragment 6 Forward Primer 51394-51415 GGGAGGAGATTCAGAGCACTCC (SEQ ID NO:318) Reverse Primer Complement of 51847-51826 CAGTCCACGTTTCCAGAACACC (SEQ ID NO:319) PCR product 454 nt Fragment 7 Forward Primer 52806-52826 GGCTTGGGATAATGGTGTTTGC (SEQ ID NO:320) Reverse Primer Complement of 53529-53507 TACTTCCCGAAGGTGGAAGAAGG (SEQ ID NO:321) PCR product 724 nt Fragment 8 Forward Primer 53242-53265 CAGTGGAGATCAGCAAGACAGTCC (SEQ ID NO:322) Reverse Primer Complement of 53807-53786 GGGCATCTCGGGTTCTACTTCC (SEQ ID NO:323) PCR product 566 nt Fragment 9 Forward Primer 53522-53544 GGGAAGTACGAGTGCTCACATGC (SEQ ID NO:324) Reverse Primer Complement of 54110-54088 CTTTATACCCCTCTTCCCCACTGC (SEQ ID NO:325) PCR product 589 nt Fragment 10 Forward Primer 53821-53841 TCTCTGAGCCAACCACTGTGC (SEQ ID NO:326) Reverse Primer Complement of 54359-54337 GGCTGAGTAGACAATGCCACTGC (SEQ ID NO:327) PCR product 539 nt Fragment 11 Forward Primer 54055-54076 CTGTGTCCCCAGAGAAATGTGG (SEQ ID NO:328) Reverse Primer Complement of 54717-54695 GACTCAGCAACAAGAGGACATGC (SEQ ID NO:329) PCR product 663 nt Fragment 12 Forward Primer 54342-54365 GGCATTGTCTACTCAGCCCTTACC (SEQ ID NO:330) Reverse Primer Complement of 54986-54967 ACAAGTCGAGGTGCCCAAGG (SEQ ID NO:331) PCR product 645 nt Fragment 13 Forward Primer 54669-54693 CCCACATACATGAGGGTCTCTTAGG (SEQ ID NO:332) Reverse Primer Complement of 55270-55250 ATTCTGCCTCCAGCATCAACC (SEQ ID NO:333) PCR product 602 nt Fragment 14 Forward Primer 55235-55258 AACAGAGCTTTCCTTTAGGTTGATGC (SEQ ID NO:334) Reverse Primer Complement of 55847-55825 CCTCAGTTCCCCACTACCTTAGC (SEQ ID NO:335) PCR product 613 nt

[0146] These primer pairs were used in PCR reactions containing genomic DNA isolated from immortalized cell lines for each member of Index Repository IA. The PCR reactions were carried out under the following conditions: Reaction volume = 20 μl 10 × Advantage 2 Polymerase reaction buffer (Clontech) = 2 μl 100 ng of human genomic DNA = 1 μl 10 mM dNTP = 0.4 μl Advantage 2 Polymerase enzyme mix (Clontech) = 0.2 μl Forward Primer (10 μM) = 0.4 μl Reverse Primer (10 μM) = 0.4 μl Water = 15.6 μl Amplification profile: 94° C. - 2 min.  1 cycle 94° C. - 30 sec. 70° C. - 45 sec. {close oversize bracket} 10 cycles 72° C. - 1 min. 94° C. - 30 sec. 64° C. - 45 sec. {close oversize bracket} 35 cycles 72° C. - 1 min.

[0147] Sequencing of PCR Products

[0148] The PCR products were purified by Solid Phase Reversible Immobilization using the protocol developed by the Whitehead Genome Center. A detailed protocol can be found at http://www.genome.wi.mit.edu/sequencing/protocols/pure/SPRI_pcr.html.

[0149] Briefly, five ill of carboxyl coated magnetic beads (10 mg/ml) and 60 μof HYB BUFFER (2.5M NaCl/20% PEG 8000) were added to each PCR reaction mixture (20 μl). The reaction mixture was mixed well and incubated at room temperature (RT) for 10 min. The microtitre plate was placed on a magnet for 2 min and the beads washed twice with 150 μl of 70% EtOH. The beads were air dried for 2 min and the DNA was eluted in 25 μl of distilled water and incubated at RT for 5 min. The beads were magnetically separated and the supernatant removed for testing and sequencing.

[0150] The purified PCR products were sequenced in both directions using the primer sets described previously or those listed, in the 5′ to 3′ direction, below. Accession Number: AC004525 Fragment 1 Forward Primer 32865-32882 GCGCTGGCCCTCAACTTT (SEQ ID NO:336) Reverse Primer Complement of 33283-33264 GTCCCTGGAGATGGGACCTC (SEQ ID NO:337) Fragment 2 Forward Primer 35598-35617 GCCCCCAGATCTGTCCTCAC (SEQ ID NO:33 8) Reverse Primer Complement of 36013-35994 GGAAAATACAGGCGGCTTCC (SEQ ID NO:339) Fragment 3 Forward Primer 37182-37203 GGCTCTGAATCTGTGTGGTGCT (SEQ ID NO:340) Reverse Primer Complement of 37639-37620 AGCCAGGTGAGAAGCCAGGT (SEQ ID NO:341) Fragment 4 Forward Primer 43266-43285 GGCCTGAACAGGACGAACAA (SEQ ID NO:342) Reverse Primer Complement of 43687-43668 GGCAGGATTGCCATTAGAGG (SEQ ID NO:343) Fragment 5 Forward Primer 49639-49660 TGAGTCAGTGGTTTGACCTCCA (SEQ ID NO:344) Reverse Primer Complement of 49999-49980 GCCTCTGTCTCCCCTGCAAC (SEQ ID NO:345) Fragment 6 Forward Primer 51423-51442 CCATTTTGCCATCGACCAC (SEQ ID NO:346) Reverse Primer Complement of 51818-51799 CTGCCGTCCCTTTGAAGGCTA (SEQ ID NO:347) Fragment 7 Forward Primer 52932-52953 CCCTACCCTCAGGGATTTCTCA (SEQ ID NO:348) Reverse Primer Complement of 53474-53455 CCCATTCTCCTCTCCGAGCA (SEQ ID NO:349) Fragment 8 Forward Primer 53280-53299 ATCAGCGTGGTGCGATGTGT (SEQ ID NO:350) Reverse Primer Complement of 53756-53737 ACCCAGCTCTCTGGGACACG (SEQ ID NO:351) Fragment 9 Forward Primer 53548-53568 GGGATGAGTTCCCAAGTGCAG (SEQ ID NO:352) Reverse Primer Complement of 54048-54029 TGGCAAGCAGGCTTGAGAAG (SEQ ID NO:353) Fragment 10 Forward Primer 53841-53860 CCCCAACCTGAGCCAGAAAC (SEQ ID NO:354) Reverse Primer Complement of 54330-54311 TGTCCACAAGGGGGTCTGTG (SEQ ID NO:355) Fragment 11 Forward Primer 54083-54102 GGCTAGCAGTGGGGAAGAGG (SEQ ID NO:356) Reverse Primer Complement of 54617-54600 ATTGCCAGGGGCAGGATG (SEQ ID NO:357) Fragment 12 Forward Primer 54422-54441 CCCTGTCATGGCCAGTCCTT (SEQ ID NO:358) Reverse Primer Complement of 54929-54910 GCGACCCAGTGCCCTCTACT (SEQ ID NO:359) Fragment 13 Forward Primer 54694-54715 TGCATGTCCTCTTGTTGCTGAG (SEQ ID NO:360) Reverse Primer Complement of 55213-55194 CAATGACCACCCTCCCTGAA (SEQ ID NO:361) Fragment 14 Forward Primer 55273-55291 CGGCTGTCAAGGGGTGTTC (SEQ ID NO:362) Reverse Primer Complement of 55769-55750 CCAAACCCAGACGGCAAGTT (SEQ ID NO:363)

[0151] Analysis of Sequences for Polymorphic Sites

[0152] Sequences were analyzed for the presence of polymorphisms using the Polyphred program (Nickerson et al., Nucleic Acids Res. 14:2745-2751, 1997). The presence of a polymorphism was confirmed on both strands. The polymorphisms and their locations in the IL4Rα gene are listed in Table 3 below.

Example 1B

[0153] This example illustrates examination of the IL4Rα gene for polymorphic sites in the following target regions: 1000 base pairs upstream of the ATG start codon; each of the exons, including approximately 100 base pairs on either side of the exon; and 500-1000 base paris downstream of the termination codon.

[0154] Amplification of the Target Regions PCR primers, which were designed based on the nearly complete IL4R genomic sequence reported in the GenBank database (Accession No: AC004525), are set forth below: Promoter Forward Primer 30094-30117 AAACCCCTGGACTCCAAGTGATCC (SEQ ID NO:364) Reverse Primer Complement of 30842-30819 AAGCGATTCTTCTGCCTCAGCCTC (SEQ ID NO:365) PCR product 749 nt Exon 1 Forward Primer 30517-30540 GGACAGTTGTTGTGTAGCTCACCC (SEQ ID NO:366) Reverse Primer Complement of 31409-31431 CTATGTTGCCCAAGCTGACCTC (SEQ ID NO:367) PCR product 893 nt Exon 2 Forward Primer 32871-32890 GCCCTCAACTTTGCCTGCAC (SEQ ID NO :368) Reverse Primer Complement of 33362-33340 AGTCCAGTATTCCAGCCGTATCC (SEQ ID NO:369) PCR product 492 nt Exon 3 Forward Primer 35623-35644 TGATCGGGAAGCTGGAAGAGTC (SEQ ID NO:370) Reverse Primer Complement of 36070-36049 CGTTTCAAAGGTGGGAGGACTG (SEQ ID NO:371) PCR product 448 nt Exon 4 Forward Primer 37230-37250 CGACCAAAAATCTGGGTGGTG (SEQ ID NO:372) Reverse Primer Complement of 37668-37648 CAGGAAGCAAAGGGACTTGCC (SEQ ID NO:373) PCR product 439 nt Exon 5 Forward Primer 43307-43328 TCTTAAACATGGTGGGGTCAGC (SEQ ID NO:374) Reverse Primer Complement of 43765-43745 CATGGAAATTTGTGGGCTTTGTG (SEQ ID NO:375) PCR product 459 nt Exon 6 Forward Primer 46507-46528 ATGTGCAAGAGGGAGAGTGGTG (SEQ ID NO:376) Reverse Primer Complement of 46870-46849 TGACTGAGAGGACTGCAAAGGG (SEQ ID NO:377) PCR product 364 nt Exon 7 Forward Primer 49672-49695 GCCTGATCTCTGATGCCAAATAAG (SEQ ID NO:378) Reverse Primer Complement of 49964-49983 TTTGCCATFCCAGAAGCCAG (SEQ ID NO:379) PCR product 293 nt Exon 8 Forward Primer 51524-51546 GATCTGTGTGATGTCGAGGCTTG (SEQ ID NO:380) Reverse Primer Complement of 51845-51825 GTCCACGTTTCCAGAACACCC (SEQ ID NO:381) PCR product 322 nt Exon 9 Fragment 1 Forward Primer 52912-52933 CGAAATCCCAAAGACACAGACC (SEQ ID 140:382) Reverse Primer Complement of 53722-53701 GAGTTGCTGAAGCTGCGGTAAG (SEQ ID NO:3 83) PCR product 811 nt Exon 9 Fragment 2 Forward Primer 53352-53374 GAAAAAGGGAGCTTTCTGTGCATC (SEQ ID NO:384) Reverse Primer Complement of 54172-54153 AACAAGGGGACAGGGACTGG (SEQ ID 140:385) PCR product 821 nt Exon 9 Fragment 3 Forward Primer 53854-53874 CAGAAACCTGGGAGCAGATCC (SEQ ID NO:386) Reverse Primer Complement of 54711-54688 GCAACAAGAGGACATGCACCTAAG (SEQ ID 140:387) PCR product 858 nt Exon 9 Fragment 4 Forward Primer 54266-54288 AAAGGTAGAGGACATGCCAAAGC (SEQ ID NO:388) Reverse Primer Complement of 55007-54987 GGAGCAGCCAACAACTCGTTC (SEQ ID 140:389) PCR product 742 nt

[0155] These primer pairs were used in PCR reactions containing genomic DNA isolated from immortalized cell lines for a reference population of 70 human individuals. The PCR reactions were carried out under the following conditions: Reaction volume = 20 μl 10 × Advantage 2 Polymerase reaction buffer (Clontech = 2 μl 100 ng of human genomic DNA = 1 μl 10 mM dNTP = 0.4 μl Advantage 2 Polymerase enzyme mix (Clontech) = 0.2 μl Forward Primer (10 μM) = 0.4 μl Reverse Primer (10 μM) = 0.4 μl Water = 15.6 μl Amplification profile: 94° C. - 2 min.  1 cycle 94° C. - 30 sec. 70° C. - 45 sec. {close oversize bracket} 10 cycles 72° C. - 1 min. 94° C. - 30 sec. 64° C. - 45 sec. {close oversize bracket} 35 cycles 72° C. - 1 min.

[0156] Sequencing of PCR Products

[0157] The PCR products were purified by Solid Phase Reversible Immobilization using the protocol developed by the Whitehead Genome Center. A detailed protocol can be found at http://www.genome.wi.mit.edu/sequencing/protocols/pure/SPRI_pcr.html.

[0158] Briefly, five μl of carboxyl coated magnetic beads (10 mg/ml) and 60 μl of HYB BUFFER (2.5M NaCl/20% PEG 8000) were added to each PCR reaction mixture (20 μl ). The reaction mixture was mixed well and incubated at room temperature (RT) for 10 min. The microtitre plate was placed on a magnet for 2 min and the beads washed twice with 150 μl of 70% EtOH. The beads were air dried for 2 min and the DNA was eluted in 25 μl of distilled water and incubated at RT for 5 min. The beads were magnetically separated and the supernatant removed for testing and sequencing.

[0159] The purified PCR products were sequenced in both directions using the primer sets described previously or those listed, in the 5′ to 3′ direction, below. Promoter Fragment 1 Forward Primer 30312-30334 GCTCATTTAATCCCCACAACACC (SEQ ID NO:390) Reverse Primer Complement of 30791-30769 CCACCACACCTGGCTAATTTTTG (SEQ ID NO:391) Promoter Fragment 2 Forward Primer 30529-30551 TGTAGCTCACCCTCTGGACTTTG (SEQ ID NO:392) Reverse Primer Complement of 30990-30971 AATATGCAACCCTCCCCTGC (SEQ ID NO:393) Exon 1 Forward Primer 30824-30846 TGAGGCAGAAGAATCGCTTGAAC (SEQ ID NO:394) Reverse Primer Complement of 31261-31240 ACTTGTCATTGGCTGTCCCCTC (SEQ ID NO:395) Exon 2 Forward Primer 32880-32900 TTTGCCTGCACTGTGCTTTTG (SEQ lED NO:396) Reverse Primer Complement of 33234-33212 CCATACTCAGCATCCTGCACTCC (SEQ ID NO:397) Exon 5 Forward Primer 43330-43349 AACGACAGCAACCAGGGTGG (SEQ ID NO:398) Reverse Primer Complement of 43704-43682 CAGCAGGTGTATCTAATGGCAGG (SEQ ID NO:399) Exon 6 Forward Primer 46520-46541 AGAGTGGTGGGGAGATGAGGTG (SEQ ID NO:400) Reverse Primer Complement of 46857-46837 TGCAAAGGGGCAGACTAGAGG (SEQ ID NO:40 1) Exon 7 Forward Primer 49708-49729 CGACCACTTTTATGGGAGGAGC (SEQ ID NO:402) Reverse Primer Complement of 49927-49905 CCAGGTGTTCTGAACCACACTTC (SEQ ID NO:403) Exon 8 Forward Primer 51528-51550 TGTGTGATGTCGAGGCTTGTACC (SEQ ID NO:404) Reverse Primer Complement of 51779-51758 GAATGCAGGGAAGAGAAGGCAG (SEQ ID NO:405) Exon 9 Fragment 1 Forward Primer 53017-53038 GCCATCAGGACATGGTGATTTC (SEQ ID NO:406) Reverse Primer Complement of 53539-53518 TGAGCACTCGTACTTCCCGAAG (SEQ ID NO:407) Exon 9 Fragment 2 Forward Primer 53378-53399 TGAGAGCAGCAGGGATGACTTC (SEQ ID NO:408) Reverse Primer Complement of 53948-53926 AAACTCCTGATAGCCACTGGTGG (SEQ ID NO:409) Exon 9 Fragment 3 Forward Primer 53869-53868 AGATCCTCCGCCGAAATGTC (SEQ ID NO:410) Reverse Primer Complement of 54583-54560 TTACTCTTCTCTGAGATGCCCGAG (SEQ ID NO:411) Exon 9 Fragment 4 Forward Primer 54334-54355 TGGGCAGTGGCATTGTCTACTC (SEQ ID NO:412) Reverse Primer Complement of 54769-54750 TTCCAGGAGGTGGCATTTCC (SEQ ID NO:413)

[0160] Sequencing reactions were performed using the Big-Dye terminator kit from PE Biosystems (Foster City, Calif.) according to the manufacturer's instructions. The sequencing products were analyzed on an ABI 477 automated sequencer (PE Biosystems, Foster City, Cailf.).

[0161] Analysis of Sequences for Polymorphic Sites Sequences were analyzed for the presence of polymorphisms using the Polyphred program (Nickerson et al., 14 Nucleic Acids Res. 2745-2751, 1997). The presence of a polymorphism was confirmed on both the strands. The polymorphisms and their locations in the IL4Rα gene are listed in Table 3 below. TABLE 3 Polymorphic Sites Identified in the IL4Rα Gene Polymorphic Nucleotide Position in Nucleotide Position in Reference Variant Site Number GenBank Accession Allele Allele Example PS1 97137(Acc#AC004525) 32884 A G 1B PS2 97118(Acc#AC004525) 32903 C T 1A PS3 97060(Acc#AC004525) 32961 G T 1A PS4 96886(Acc#AC004525) 33135 G C 1A PS5^(R) 94272(Acc#AC004525) 35749 A G 1A, 1B PS6 94258(Acc#AC004525) 35763 C T 1A, 1B PS7 94251 (Acc#AC004525) 35770 G A 1A P58 94204(Acc#AC004525) 35817 T C 1A PS9 94116(Acc#AC004525) 35905 C T 1B PS10 94077(Mc#AC004525) 35944 C T 1A PS11 94063(Acc#AC004525) 35958 G A 1B PS12 92691(Acc#AC004525) 37330 C A 1A PS13 92548(Acc#AC004525) 37473 C T 1A P514 92435(Acc#AC004525) 37586 C T 1A PS15 92430(Acc#AC004525) 37591 C A 1A PS16 92417(Acc#AC004525) 37604 A T 1A PS17 92377(Acc#AC004525) 37644 C A 1A PS18 92343(Acc#AC004525) 37678 C T 1A PS19 86575(Acc#AC004525) 43446 G A 1A PS20 86318(Acc#AC004525) 43703 T C 1A PS21 77013(Acc#AC004525) 53008 A C 1A PS22 76922(Acc#AC004525) 53099 C T 1B PS23 76868(Acc#AC004525) 53153 T C 1A PS24^(R) 76608(Acc#AC004525) 53413 A C 1A PS25 76565(Mc#AC004525) 53456 C T 1A, 1B PS26^(R) 76516(Mc#AC004525) 53505 T C 1A, 1B PS27 76514(Acc#AC004525) 53507 C T 1A P528 76508(Acc#AC004525) 53513 T C 1A PS29^(R) 76300(Mc#AC004525) 53721 T C 1A, 1B PS30 76106(Acc#AC004525) 53915 C T 1A PS31^(R) 76080(Acc#AC004525) 53941 A C 1A, 1B PS32 76072(Acc#AC004525) 53949 G A 1A PS33 75784(Acc#AC004525) 54237 C T 1A PS34 75553(Acc#AC004525) 54468 T C 1A, 1B PS35 75410(Acc#AC004525) 54611 T C 1A PS36 75323(Acc#AC004525) 54698 T C 1A, 1B PS37 75321(Acc#AC004525) 54700 T C 1A PS38 75280(Acc#AC004525) 54741 C T 1A PS39 75241(Acc#AC004525) 54780 C G 1A PS40 74938(Acc#AC004525) 55083 A G 1A PS41 74879(Acc#AC004525) 55142 G A 1A PS42^(R) 74693(Acc#AC004525) 55328 G A 1A PS43^(R) 74591(Acc#AC004525) 55430 C T 1A PS44 74482(Acc#AC004525) 55539 C T 1A PS45 14263(Acc#AC004525) 55758 G A 1A

Example 2

[0162] This example illustrates analysis of the IL4Rα polymorphisms identified in the Index Repositories for human genotypes and haplotypes for all polymorphic sites except PS1, PS9, PS11, PS21, PS22, and PS23.

[0163] A sampling of different genotypes containing these polymorphisms that were observed in these reference populations are shown in Table 4 below, with the haplotype pair indicating the combination of haplotypes determined for the individual using the haplotype derivation protocol described below. In Table 4, homozygous positions are indicated by one nucleotide and heterozygous positions are indicated by two nucleotides. Missing nucleotides in any given genotype in Table 4 can typically be inferred based on linkage disequilibrium and/or Mendelian inheritance. TABLE 4 Genotypes and HAP Pairs Observed for the IL4Rα Gene PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS 2 3 4 5 6 7 8 10 12 13 14 15 16 17 18 19 20 24 25 26 27 28 29 30 31 32 33 34 35 36 1 C G G A C G T C G C C G A C G T A G T C T T C A G C T T T 2 C G G A C G T C G C C G A C C G T A G T C T T C A G C T T T 3 C G G G/A C G T C/T G C C G A C C/T G C/T A G T C T T C A/G G C T T T/C 4 C/T G G G/A C G T C G/A C/T C G A C C G C/T A G T C T T C A G C T T T 5 C G G G/A C G T C/T G C C G A C C/T G C/T A G T C T T C A G C T T T 6 C G G A C G T C G C C G A C C/T G C/T A G T C T T C A/G G C T T T/C 7 C G G A C G T C G C C G A C C/T G C/T A G T C T T C A G C T T T 8 C/T G G G/A C G T C/T G C C G A C C/T G C/T A G T C T T C A G C T T T 9 C G G A C G T C G C C G A C C G T A G T C T T C A G C T T T 10 C G G G/A C G T C G C/T C G A C C G C/T A G T C T T C A G C T T T 11 C G G G/A C G T C/T G C C G A C C/T G C/T A G T C T T C A G C T T T 12 C/T G G G C G T T G C C G A C T G C A/C G/T T/C C T/C T/C C G G C T T T/C 13 C G G G C G T T G C/T C G A C C G C/T A/C G/T T C T/C T C A/G G C T/G T T 14 — — — G/A C G T C/T G C C G A C C/T G C/T A/C G/T T/C C T/C T/C C A/G G C T T T 15 C G G G C G T T G C C G A C T G C C T C C C C C G G C T T T 16 C G G G/A C G T C G C C G A C C G C C T T/C C C C C G G C T T T 17 C G G G C G T C G C C G A C C G C A G T C T T C G G C T T T 18 C G G/C G C G T T G C C G A C C/T G C C T T C C T/C C G GT C T/G T/C T/C T/C 19 C G G G/A C G T C/T G C C G A C C/T G C A/C G/T T C T/C T/C C G G C T T/C 20 C/T G G G/A C G T C G/A C/T C G/A A C C G C/T A G T C T T C A G C T T T T 21 C G G A C G T C G C C G/A A C/A C G C/T A/C G/T T/C C T/C T/C C A/G G C T T T 22 C G G G C G T C G C/T C G A C C G C C T T C C T/C C G T C T/G T T 23 C G G G C G T T G C C G A C T G C A G T C T T C A/G G C T T T/C T 24 C G G G/A C G T C G C C G A C C G C A/C G/T T C T/C C C G G C T/G T T 25 C G G A C G T C G C C G A C C/T G C C T T C C T/C C G G/A C T/G T T T/C 26 C G G A C G T C G C C G A C C/T G C C T T/C C C T/C C G G/A C T/G T T 27 C/T G G G C G T C/T G C C G A C C/T G C A/C G/T T C T/C T C G G/A C G T T/C 28 T G G G C G T C G C C G A C C G C A G T C T T C G G — G T C 29 C/T G G G C G T C/T G C C G A C C/T G C A G T C T T C A/G G C T/G T T/C 30 C G G A C G/A T C G C C G A C/A C G C/T A/C G/T T/C C T/C T/C C A/G G C T T T 31 C G G G/A C G T C/T G C C G A C C/T G C/T A G T C T T C A G C T T T 32 C/T G G G C G T T G C C G A C T G C A/C G/T T/C C T/C T/C C A/G G C T T T 33 C G G G C G T T G C C G A C T G C A/C G/T T C T/C T C A/G G/A C T/G T T 34 C G G G/A C G T C/T G C C G A C C/T G C/T A G T C T T C A/G G C T T T T 35 C G G G/A C G T C/T G C C G A — — G C/T A G T C T T C/T A G C T T T 36 C G G G/A C G T C/T G C C G A — — G C A G T C T T C A G C T T T T 37 C G G G C G T T G C C G A C T G C A G T C T T C A G C T T T 38 C G G — — — T T G C C G A C C/T G C/T A G T C T T C A G C T T T 41 C G G G C G T T G C C/T G A C C G C/T A/C G/T T C T/C T C A/G G C T/G T T/C 42 C/T G G G/A C/T G T/C C G C C G A C C G C C T T C/T C T/C C G G C T/G T T/C PS PS PS PS PS PS PS PS PS HAP 37 38 39 40 41 42 43 44 45 PAIRS T C C A G G C C G 2 2 T C C G/A G A/G C C A/G 2 3 T C C A G G C C G 2 4 T C C A G G C C G 2 15 T C C A G G C C G 2 16 T C C A G G C C G 2 36 T C C A G G C C G 2 39 T C C G/A G A/G C C A/G 2 48 T C C G/A G A/G C C A/G 3 2 T C C G G A C C A 3 24 T C C G G A C C A 3 44 T C C G/A G A/G C C G 4 5 T C C G G A C C A 4 46 T C C A G G C C G 7 2 T C C A G G C C G 7 7 T C/T C G G A C C A 9 10 T C C A G G C C G 12 12 C C G G A T C A 13 14 T T/C C C G/A G A/G C/T C A/G 13 38 C C A G G C C G 15 51 T C C A G G C C G 17 22 T C/T C G G A C C — 21 10 C C G/A G G C C G 23 4 T/C C C/G G G A C/T C A 28 31 C C G G A T C A 29 37 T C C G G A/G C/T C A/G 32 33 T/C C C G G A C/T C A 41 8 C C C G G A C C A 41 41 T/C C C G G A C C A 41 44 T C C A G G C C G 43 22 T C C G G A C C A 44 3 T C C G A C C A/G 44 5 T C C G G A C/T C A 44 8 C C G G A C C A 44 30 T C C G/A G A/G C C A/G 44 34 C C G G A C C A 44 40 T C C G G A C C A 44 44 T C C G G A C C A 44 46 T C C G G A C/T C A 46 50 T C C G G A T C A 53 20

[0164] The haplotype pairs shown in Table 4 were estimated from the unphased genotypes using an extension of Clark's algorithm (Clark, A. G. (1990) Mol Bio Evol 7, 111-122), as described in U.S. Provisional Patent Application filed Apr. 19, 2000 and entitled “A Method and System for Determining Haplotypes from a Collection of Polymorphisms”. In this method, haplotypes are assigned directly from individuals who are homozygous at all sites or heterozygous at no more than one of the variable sites. This list of haplotypes is then used to deconvolute the unphased genotypes in the remaining (multiply heterozygous) individuals.

[0165] By following this protocol, it was determined that the Index Repositories examined herein and, by extension, the general population contains the 53 human IL4Rα haplotypes shown in Table 5 below. TABLE 5 A. Haplotypes Observed for the IL4Rα Gene HAP PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS ID 2 3 4 5 6 7 8 10 12 13 14 15 16 17 18 19 20 24 25 26 27 28 29 30 31 32 33 34 35 36 1 C G G A C G T C G C C G A C T G C A G T C T T C A G C T T T 2 C G G A C G T C G C C G A C C G T A G T C T T C A G C T T T 3 C G G A C G T C G C C G A C C G T A G T C T T C A G C T T T 4 C G G G C G T T G C C G A C T G C A G T C T T C G G C T T C 5 T G G G C G T T G C C G A C T G C C T C C C C C G G C T T T 6 C G G G C G T T G C C G A C T A C A G T C T T C A G C T T T 7 C G G G C G T T G C C G A C T G C C T C C C C C G G C T T T 8 C G G G C G T T G C C G A C T G C C T T C C T C G A C G T T 9 C G G A C G T C G C C G A C C G C C T C C C C C G G C T T T 10 C G G G C G T C G C C G A C C G C C T T C C C C G G C T T T 11 C G G A C G T C G C C G A C C G C A G T C T T C G G C G T C 12 C G G G C G T C G C C G A C C G C A G T C T T C G G C T T T 13 C G G G C G T T G C C G A C T G C C T T C C C C G G C T C T 14 C G C G C G T T G C C G A C C G C C T T C C T C G G C G T C 15 T G G G C G T C A T C G A C C G C A G T C T T C A G C T T T 16 C G G G C G T T G C C G A C T G C A G T C T T C A G C T T T 17 C G G A C G T C G C C A A C C G C C T C C C C C G G C T T T 18 C G G A C G T C G C C G A A C G C A G T C T T C A G C T T T 19 C G G G C G T C G T C G A C C G C C T T T C C C G G C G T C 20 C G G A C G T C G C C G A C C G C C T T T C C C G G C T T T 21 C G G G C G T C G T C G A C C G C C T T C C T C G G C G T T 22 C G G A C G T C G C C G A A C G T A G T C T T C A G C T T T 23 C G G G C G T T G C C G A C T G C A G T C T T C A G C T T T 24 C G G G C G T C G T C G A C C G C A G T C T T C A G C T T T 25 T G G G C G T C A T C G A C C G C C T T C C C C G G C T C T 26 C G G G C G T T G C C G A C T G C C T T C C T C G G C G T C 27 C G G G C G T T G C C G A C T G C A G T C T T C A G C T T T 28 C G G A C G T C G C C G A C C G C A G T C T C C G G C G T T 29 C G G A C G T C G C C G A C C G C C T T C C C C G G C T T T 30 C G G A C G T C G C C G A C C G T A G T C T T C G G C T T T 31 C G G G C G T C G C C G A C C G C C T T C C C C G G C T T T 32 C G G A C G T C G C C G A C C G C C T T C C T C G A C G T T 33 C G G A C G T C G C C G A C T G C C T C C C C C G G C T T T 34 C G G A C G T C G C C G A C C G T A G T C T T T A G C T T T B. Haplotypes Observed for the IL4Rα Gene HAP PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS PS ID 2 3 4 5 6 7 8 10 12 13 14 15 16 17 18 19 20 24 25 26 27 28 29 30 31 32 33 34 35 36 35 C G G A C G T C G C C G A C C G T A G T C T T C A G T T T T 36 C G G A C G T C G C C G A C T G C A G T C T T C G G C T T C 37 C G G A C G T C G C C G A C T G C C T T C C T C G A C G T T 38 C G G A C G T C G C C G A C C G C A G T C T T C G G C T T T 39 C G G A C G T C G C C G A C T G C A G T C T T C A G C T T T 40 C G G A C G T C G C C G A C C G C A G T C T T C A G C T T T 41 T G G G C G T C G C C G A C C G C A G T C T T C G G C G T C 42 C G G A C A T C G C C G A C C G T A G T C T T C A G C T T T 43 C G G A C A T C G C C G A C C G C C T C C C C C G G C T T T 44 C G G G C G T T G C C G A C T G C A G T C T T C A G C T T T 45 C G G G C G T T G C C G A C C G T A G T C T T C A G C T T T 46 C G G G C G T T G C C G A C C G T A G T C T T C A G C T T T 47 C G G G C G T T G C C G A C T G C C T C C C C C G G C T T T 48 T G G G C G T T G C C G A C T G C A G T C T T C A G C T T T 49 C G G G C G T T G T C G A C C G C C T T C C T C G G C G T T 50 C G G G C G T T G C T G A C C G C C T T C C T C G G C G T C 51 C G G A C G T C G C C A A C C G T A G T C T T C A G C T T T 52 T T G G C G T T G C C G A C T G C C T C C C C C G G C T T T 53 T G G G T G C C G C C G A C C G C C T T C C T C G G C G T C A. Haplotypes Observed for the IL4Rα Gene PS PS PS PS PS PS PS PS PS 37 38 39 40 41 42 43 44 45 T C C G G A C C A T C C A G G C C G T C C G G A C C A T C C A G G C C G T C C G G A C C G T C C G G A C C A T C C A G G C C G T C C G G A T C A T C C G G A C C A T T C G G A C C A C C C G G A C C A T C C A G G C C G C C C G G A T C A T C C G G A T C A T C C A G G C C G T C C A G G C C G T C C A G G C C G T C C G G A C C A T C C G G A T C A T C C G G A T C A T C C G G A C C A T C C A G G C C G T C C G G G C C G T C C G G A C C A C C C G G A T C A T C C G G A T C A T C C G G A T T A C C G G G A T C A C C C G G A T C A T C C G G A C C A T C C G G A C C A T C C G G A T C A T C C G G G C C G T C C A G G C C C B. Haplotypes Observed for the IL4Rα Gene PS PS PS PS PS PS PS PS PS 37 38 39 40 41 42 43 44 45 T C C G G A C C A T C C A G G C C G T C C G G A T C A T C C A G G C C G T C C A G G C C G T C C G G A C C A C C C G G A C C A T C C G G A C C A T C C A G G C C G T C C G G A C C A T C C A G G C C G T C C G G A C C A T C C G G A C C G T C C G G A C C A T C C G G A C C A T C C G G A T C A T C C A G G C C G T C C G G A C C G T C C G G A T C A

[0166] In view of the above, it will be seen that the several advantages of the invention are achieved and other advantageous results attained.

[0167] As various changes could be made in the above methods and compositions without departing from the scope of the invention, it is intended that all matter contained in the above description and shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.

[0168] All references cited in this specification, including patents and patent applications, are hereby incorporated in their entirety by reference. The discussion of references herein is intended merely to summarize the assertions made by their authors and no admission is made that any reference constitutes prior art. Applicants reserve the right to challenge the accuracy and pertinency of the cited references.

1 413 1 28690 DNA Homo sapiens 1 tgtgagctac tgtgtctggc ctgaataata aaatttaaaa caatttttca aaaattcacc 60 atgaggtctc actatattcc ctaggctggt ctcaaacccc tggactccaa gtgatccacc 120 ccaccttccc gagtagctgg gactagagat gcacaccatt gcacccaata gagcaatacg 180 tttctgttct ttgtaaatta cctgctctaa ggtatttttg ttatagcagc ctatatggac 240 taagctgact tgtaacgtta cttgagactt taaagtgttc cggtcactgt tggagggctc 300 tgtctgtgtt agctcattta atccccacaa cacctcaatc agatggggct attcttagtc 360 ccactttata gataaggaaa ctgaggcatg gaagcacagc ttgctcaagg ttcacatcta 420 gtcagtgaca gagcaggtat ttaaacctca ggaaataatc agagaaacat gtgtagaggg 480 ttgtccaagg aaggccacat ccagaagcat ctcccaggac agttgttgtg tagctcaccc 540 tctggacttt gtgggtctgg gtgttgtttc atgattatag agagagctct gtgaacgtgg 600 aggacctgtt gtcggcagag acacaaatgg ccagggcatg gctgggcagc cgcagtggct 660 caggcctgta atcccagcac ttcgagaaga ccagaggggc agatcatgag gtcagaagtt 720 caagaccagc ctggccaaca tggtgaaacc ccgtctctac taaaaataca aaaattagcc 780 aggtgtggtg gtgggcacct gtaatcccag ctactcggga ggctgaggca gaagaatcgc 840 ttgaacccgg gaggtggagg ttgcagtgag ctgagattgc accactgcac tccagccttg 900 gagacagagc gagactctgt ctcggaaaaa caaacaaaca agcaaacaaa caaacaaata 960 aatggccagg gcaggggagg gttgcatatt gaataagatg agctctgctg gaagcacagg 1020 tcagcactaa cctgcttcct ctctctctgc aggtgccttg gcatctccca atggggtggc 1080 tttgctctgg gctcctgttc cctgtgagct gcctggtcct gctgcaggtg gcaagctctg 1140 gtaagtcacc acttctcaat cattcatttg ttggctatta atggcgtgcc agggtcctgc 1200 agtatgtcac ctggccttat ggagattaca ctgcagtggg aggggacagc caatgacaag 1260 tggccctgat tatcagtaaa ttctaaagat tgttagaaag tgatgggagc cgggtgcagt 1320 ggctcacacc tgtaatccca gcacttcagg aggccgaggc aggaggatcg cttgagccca 1380 ggagttcgag gtcagcttgg gcaacatagg gagaccttgt ctctacaaat aataaaatat 1440 tagccaggtg tggcagtgca cgcctgtagc cccagctact caggaggccg aggtgggagg 1500 atcccttgaa ctcaggaggt caaggctgca gtgaactgtg atcgcgccac tccactccag 1560 cctgcgtgag aaagtgagac cctgtcaaaa aaaaagagaa ggtgatgggg aaagaacaca 1620 gaacagcata agagggggtt ggggaagctg ggtggagtgg gggggattgc agttgaaagt 1680 agggaagtca gggaaggcct cattgagctg acttggagga agcgggaacc gtgcagatgt 1740 ctggggaagg ctcattcttg gcagagaggc cctgcactga gcctggcggg agggttgagc 1800 acaggaggga atgtggtgga ggagagtgag cagcaggagg gagcagtgaa ggtcagcaag 1860 gtgacagagt ggctgaatca aaaaagacct tgcagtgttt gagcagagga tccatatcat 1920 ccattatgtt ccaaaggact cttcaggatg ccgtgtggag aaaggaagag ggtggaagcc 1980 aggaggtctg gagggaggtc tggagtggag gagatgagag gctccggatc cctctgggag 2040 gtagatttga ggacagattg gaattgaggt gaaagacaga gaaagagaag tggccaggat 2100 gactccaaga tttctgacct aaactactgg gaaggacgcg gttgtcattt ctgaaatgca 2160 gaaggatgcc agaagagaag gtactttggg gaggggcggg aatcaggagt tagttttgga 2220 catgagataa gcttggaata tttatttgct atctaagaca gctccttaac atggtaagcc 2280 cttatgcaag ttgttgtcag ctgagatggg cgtggcactg agcatgggag catggaggcg 2340 cctgagtggt ctcatgctca ggtggtttag caaactcagt gtacatcctg ccaattccag 2400 tcctgccatg gccactgaca agctaggagg gcgctgaaag gagaaggacc ccgatgtctc 2460 ctccagccca tccatctcct ctctcccatt ggccaaaccc aaccggaaac taaaggccaa 2520 gggtacccgg tgatgaagac tgtggtatca gcctcctgag cacagagagg gcagaaaggg 2580 gtggagacaa agaggggcgc agatagtggg caaatgggga agtggcactt cccctagctc 2640 gagggcagag gcttggtgtg atggaatggc actccttaaa ctgctacata ttttcccttt 2700 aatttggcca agaacaagtt gtcaagtttg tgtgagataa aggtgcactt ggttcgttct 2760 tgtctaatgg cccccgcacc catgggtatt tcttcagctt ccacagtcat cccgacacta 2820 gctgggaagc tccagcagcc ctggtcctgg ccccagctct gtgggcgctg gccctcaact 2880 ttgcctgcac tgtgcttttg tgctattccc cttggtcctg tttgggtgca agtccccctc 2940 acgcattgag ttcctgggcc gctcaggctg ctcctgtgtc tccccaggga acatgaaggt 3000 cttgcaggag cccacctgcg tctccgacta catgagcatc tctacttgcg agtggaagat 3060 gaatggtccc accaattgca gcaccgagct ccgcctgttg taccagctgg tttttctgct 3120 ctccgagtaa gcctgcgctg gagctggagg tttggggagg ttgtgcccaa agggtttgcc 3180 ccaagagtga gctgggtcca ggtggtgcgc tggagtgcag gatgctgagt atggtttgct 3240 gctgtttata tggtgttaga ggggaggtcc catctccagg gacatgttat gtaagataca 3300 gtggagcgca tggtgggagt gttggtccac gtggcacatg gatacggctg gaatactgga 3360 ctagaccagc agttctcaca ctttttggtc tcaggaccct ttttcacact taaaaatgag 3420 tgaggaccca aagggctttg gtgtaggtaa cacatcattc tatgtttacc taattagaac 3480 ttgcaatgaa gaaatggtgt aatttttaaa aaattaaaac aattaaaaat tttttttctt 3540 actgaaatgg aggtctcact gtgttgccca ggctgctctc aaactcctgg gctccagtga 3600 tcctcctgcc tccgcctccc aaagtgctgg gattacaagc gtgagccgct gtatccggcc 3660 caaaatggag aaattttaag tcccaacaac atgcaagccc gcattcaaca aatcttcaga 3720 tcaattacat gatcacaggt catgtagcct ctagaaaatt ccactgtacg ccagtgagag 3780 agagtgaaaa ggcaaataac gtccctgtat tatgatgaaa agagttttac ctggtgggcc 3840 cagaccacac tttgagaacc actggactag acccttgatt gaggagtacg gtgttgagag 3900 tggagtcctc tgtgatggtg gatggaccag gacacatggc ataggagtca ggtggttccc 3960 tgggctactc catggtgcac aggatgcttc gttacactgg tgcccaggac ataatcacgt 4020 acacaagaca cacagttacg gggcagactg gggatatacg gcacaccagc atgcagcgtt 4080 caccagtaaa ggtggtattc catgattatt ctaaggtaga tgggctgtgc tttgtttcca 4140 ttggcttagt ccagggattg gcaaactatg gcccgtgagc caaatccggc ccactgcttg 4200 tttttgtaaa taaagtttta ttggaacaca ctggctgctg tagttgtaac agaaactgca 4260 tggccctcct ttatgttttt tgtttgtttg tttgtttgtt tgttttcttt gagacagagt 4320 ttcgctcttg ttgcccaggc tggagtgcag tggcacaatc tcggctcact gcaacctctg 4380 cctcccgggt tcaagcgatt ctcctgtctc agcctcccga gtagttggga ttaatggtgc 4440 ctgccaccac acccggctaa tttttcgtat ttttagtaga gaccggtttt catcatgttg 4500 gccaagctgg tctcgaactc ctgaactcag gtgatccacc cgcctcagcg tcccaaagtg 4560 ctgggattac aggcatgagc cactgagccc ggcctcctcc tttatcttaa ttgaaataat 4620 tcagaaatgg aaagtcaaat actgcatgtt ctcacttata agtaagagtt aaataatgtg 4680 tacacatggg cattattcca tgtaccatgg aataacagac attgaagact tgggagggtg 4740 ggagaggggt gaaggaagag aagttactta atgggcatag tgtacaccat ttgggtgacg 4800 gacccaccag aaccccagac ttcaccacta ggcagcatat ccagtgagaa cagatctgag 4860 gcttgccatc aaaattgcac ttgtaaggcc gggcactgtg gtggctcgcg gctgtaatcc 4920 cagccctttg ggaggccgag gtgggcagat cacttgaggt caggagttcg agaccggcct 4980 ggccaacatg gtgaagctcc atctctacta aaaatacaac aattaactgg gtgtagtggc 5040 gcacacctgt aatcccagct actagggagg ctgaggcggg agaattgctt gagcccagga 5100 ggtggaggtt gcagtgagcc gagatcacat cactgtactc tagcctgggt gacagtgaga 5160 ctttgtctca ggaaaaaaaa acaaaaacaa aaaacaaaaa actcgtaccc cctaaattta 5220 tacaaataac caaaaaaaaa aaaaaaaaag gaaattgtgt ggcctttgaa gtccaaaata 5280 ttaactatct ggcctgttac agaaaaagtt tgcagacccc tggcctagcc cgtgagatgt 5340 gggttggctg ttaaggtgga acattggaat tatcttacga tggccaaact gtgcgatgca 5400 gagcttatgt tgttctaaat taattagtgc caccggttct tccctttcat gggctttcag 5460 gaacaagcta agtcccagga ccagggccgg cagctaggca ggtgtgagga gcatccttgg 5520 tgcatgtggt aagaggctgt ggccagcaag agaggcaacc ctagtcggct gccccagcac 5580 accctggccg ctcccaagcc cccagatctg tcctcacatc cgtgatcggg aagctggaag 5640 agtctgatgc ggttcctgga ggcatgtccc ggacacagct gtggggccca gccagcctac 5700 aggtgaccag cctaacccag cccctgtgtc tgcagagccc acacgtgtat ccctgagaac 5760 aacggaggcg cggggtgcgt gtgccacctg ctcatggatg acgtggtcag tgcggataac 5820 tatacactgg acctgtgggc tgggcagcag ctgctgtgga agggctcctt caagcccagc 5880 gagcatggtg agcagggcgg agtgcggcag gggtggctgg gtgtgttccc acagctgcct 5940 gggctgaggg tggggtgggc aggggaggag gtggggtcat agcaacagca ggaggaagcc 6000 gcctgtattt tcccaaatct gatgggattc ctgcccctgc ctgggcctca gtcctcccac 6060 ctttgaaacg gagctggtcg cagtagacca ccaagccccc ttcagcccag ctgtttccac 6120 ccctgaactt aagtgcccag gaaggcgtat tgagatgagg tgtgcttgct ggaaggcatg 6180 cctgctgctg attgaaaacc gaactgggaa cattccttcc attctgtgtc cactggtcag 6240 ctgctgcggc tttggatggt cttgaccgtg gaaggctgac cttcttctgg tacccggagt 6300 ccctgcagga atcccccttg agcttgctgg gctgtggtga caggagttta aaacatgcgt 6360 tgtattccag tgatgcatga tatgacatgc atcacaggaa taaaaacctg aggtctcatg 6420 gatatgattg cttcaaagga gaccaagttt taaaacagat gaatcaaaat aaagaaaaat 6480 actcagtaaa tcatcataaa gtacagagat gtggccaaag gtgtgaagga tgcagctgta 6540 aaagctgaag tttgaggccg ggtgtggtgg ttcatgccta taatcccagc actttgggag 6600 gccgagccca gcggatcacc ggaggtcagg agttcgagac cagcctggac aacatggtaa 6660 aaccccgtct ctactaaaaa tacaaaaaat tagtctggca tggtggcagg cgcctgtaat 6720 cccagctact tgggaggctg aggtaggaga atggcttgaa cccaggagaa ggaggttgca 6780 gtgagcttag atcatgctac tgccctccag cctgggcgac agagtgagat tacgtctcaa 6840 aaaaataaaa ataaataaaa ataaaaagat tttttaaaag gctgaagttt gggttacttt 6900 ggctcataca ctttgccttc actgtagaaa ggtggttagt aaagaccagg cgcggtggct 6960 catgcctgga atcccagcac tttgggagcc cagcgcaggc agatcacttg agccctgggc 7020 tattgaggct gcagtgagct gggattgtgc cactgcactc cagcctgggc aacagagtgg 7080 gaccctgtct caaaaaagaa gaaaaaaagg gtaattaata aacactaaag ttctatgtag 7140 aattttagca acattattgt tattataatc ttctttgcta tggctctgaa tctgtgtggt 7200 gctccagaag tatgctatgg aggttttgtc gaccaaaaat ctgggtggtg gctgtggttt 7260 gtaggccggg gctgggctgg gtgatggggg agtcactgca tagatcctca catagaggcc 7320 gcttctcccg cagtgaaacc cagggcccca ggaaacctga cagttcacac caatgtctcc 7380 gacactctgc tgctgacctg gagcaacccg tatccccctg acaattacct gtataatcat 7440 ctcacctatg cagtcaacat ttggagtgaa aacgacccgg cagatgtgag tgggcatgct 7500 ttgacgtttt tctgtgacct ctggggaaca gggtgggtga ccagcagagg cccagtccct 7560 ggagccagga gcctgggagg caagccctgg ggctggatag caaatcccag gagctagaga 7620 cctggcttct cacctggctc tgccctaggc aagtcccttt gcttcctggc cccccacccc 7680 tcacatcaga gaaggggagt tatctctgca tgccgctcct cctctgtaaa ggtagggctg 7740 tgggccacat ctgtgtttcc cagtttgggg gacacaagtg atcgtaggtg gcacattgac 7800 agctcacttg aataacccta ttattgaaga gaataatact gactcaagag acagtgaccc 7860 gtgtcagttc ccttttgagg ccaacgggtt aaggaggaag tccccataca gctgactcgt 7920 ttactaattc ctcttaatga agagagcaga ggccacaccc caggcttaga ctttcccaag 7980 aaaacaagat cagtttgttg gttgttcccc atggaagctg gtcctgacat tcccttcaca 8040 gtagtgttgg tggagttttt gttgttgttt gttttgagac agagtctcac tctgtcaccc 8100 agggtggaac acagtggcgt gatcttggct cactgcaacc tccgcctcct gggttctagc 8160 gattctcctg cctcagcctc ctgagcagcc gggactacag gcacctgcca ccgtgcccag 8220 ctaatttttg tatatttagt agagatgggg tttcactgcg ttggccaggc tggtctcaaa 8280 ctcctgacct cagatgatcc actcgccttg gcctcccaaa gtgctgggat tacaggtgtg 8340 agccaccgca cctggccagt ggagttcctt cttaagtaca tgtattgaca tctttaaaaa 8400 gggcgagagg atttacagga aactatcagg tcagtaatgg caggggccgt ccacagtggg 8460 tggctgagtc cccctatttt tctgctggtg tgcagggagg tcatttcctg ccacccatgt 8520 ttccccaccc tgaatccacc ttcctcacat tcccattgga gggacaatct ctggacatat 8580 gggacctggg gtcccacagg gctgcaatcc aatgcctgct gtgccactcg ccagctgtgt 8640 gatgttgggc atatcccata acctctttgt gcctcagttt cctcatctgt aacacaggag 8700 tgacaagagc acccgcccac agggctatga cagtacaagg tgtgtgatac agatgagctc 8760 ccctgtttgg cccacatgtg tcctaaaagc catgtgccct ttctcttgag tgccccaggc 8820 cacagagatc cccatctgcc cgctgtccca cacactggtc tgtcatttgt tccttgaggt 8880 ttgtgagggc cggctctgtg catcccaggg gcccaggctg ggcctggttg gctctcaggg 8940 agcaggcacc cgccacctta agctcccatg ctggtgtctg tcactgcttc ctctcaatct 9000 ggccaagcca ggggtgtcga tttatatctc tcaggtctgg tttccccttt ggcactgggc 9060 caggtatggg gaaagagcag gaatggggca gttggctcac acagcagagg ctcagaaagc 9120 ggggggcatg gggggaagga gtgcacagat gctagagagt ggggcaagtt ttgtttggtc 9180 aataaatctc cttctcatgc cccaggcctg tgcaagacct acagagagtc ccaaggatgg 9240 gctgggggga agagaaaggt accaccttca gagtccaaag atatgttatt taatattttc 9300 atatttctag atctgccttc aggcatggct ggatccagct tctaggaacc tgtccagctc 9360 tgcgccctgc tttattctgt attggcttcg tttttaggca ggctcttccc tcatgtagtg 9420 gcagatatgc ctactagttg ctccaggcct acatcccaaa gccacagtgg gaaaagggtt 9480 ttttttcttg acggttctaa taagagtcct aaggctgctg ctcagtggcc tggcttcgat 9540 gctgtgccag cctctgaacc aatcactggc tgtgggtgga gagagggtgc tggtggaggg 9600 ccctgcttgt ccagggagga gtcacatacc tgcctctagg gctgcaggtg ggctcagctc 9660 catccaaacc agatgaactg aaaataaggc aggagtggct tccccagggg aaactgggga 9720 agaggaagca ggactgtgct ggctaaaatg ccagccaggt ttaagacgtg gcaccagatg 9780 ccagtcatgg gattggattg gtcagcatgc ctgggctatg gcttaggggt atgttggtgc 9840 tcagggatgc cacaggcctc cagataccag gtctgaggca gaagaatgaa gtccagcttc 9900 tcttgtgggt ggaacagtgg caactgagat accccatctc tcccttccca agaacagagc 9960 tgaacataaa gaatttagtg attggccaga gcttggccac atgctcccct ctgatgaatg 10020 ataggccagg tgatgggatt ggcacaattg gcttagacta atgagggttg gccctggagt 10080 tgcaggcagt ggagttctgt cctaagcagt gggcacctaa acccgatggc ataaaagctg 10140 ggcgggtgtc cacctgcatc tgccacagca ctataggcac caactgtggc tcatactgag 10200 tgggataaat tccagaaaga aacattagga acttactata gaattttggg gctagagcta 10260 ctcattcatt cccctagata atttctaggc aaggttccat agtggagggg gagttttggc 10320 ttgggcattg aaggatgcat aggagttttc tagatgggga aagaagggaa cggtagacca 10380 ggcagaggga actgcatgat aaaaggttta tgggtgtgaa aattcatgga atgtttgagg 10440 attatggggt tgggggatgt gggaatatgt gtagcgataa agcaccaaac aaagccaaaa 10500 gtttagttag agccctgaat gcctgcctca taatggtttc catattttat atgcctacta 10560 tgtgccaggc acattgctca gggtcacaca gctggaaatg gcagggctga gtttttgttg 10620 ttgttgttgt tgttgagaca gagtctcact ctatcaccca ggctggaatg caggggcgtg 10680 atcatggctc actgcatcct tgacttcctg ggatcaggtg attctcccac ctctgcctcc 10740 caggtagctg ggactacagg cacaggccac cacgccaggc taattttttg tatttttagt 10800 agcgacaggg tctcgccatg ttgtccgggc tggtctggat ctcctggctt caagtgatcc 10860 ccctggctca gcctcccaag gtgctgggat tacaggcttg agccaccgca tccagcccag 10920 atctgagatt tgcacccagt atttgaactc ccaagcctgt gctctttttc ctcccatgga 10980 catttctctc agagatggtc tcccaaacac ctgtccttct tgttaaaaaa cagacaaacc 11040 gcaagtagtt ctttggaagc tcagatttct cttttgtttc ttagtaaaac atttcccagt 11100 tcccagctcc cttccagggt gtaagatttc ttcggtaact tacatctagc tgttgcttct 11160 tgtttgctca tgtttagaaa gaaagacaaa agagagtgag aattttctct cccttcccca 11220 gtctccccac aactcacacc ccaccctcag ctccctctgt aataggaaaa tctctgaact 11280 ctctgtagtt gctccagcaa tcttttggaa ctttgcttct ttcttgtgaa aaaacctccc 11340 cttggctcac tttgcaccag gtttccccaa atgtgcttcc aaccacaagc agaaatggag 11400 ctgccagtaa ccaggaagaa actgccgggg gctgaggaag aggagaggga ggtgcatagc 11460 cctggatctc gcagggagag gggtgacagg atgagaactc aggttgctca cttgccatca 11520 gggtcagtca tgaatatagc gttcatgtat cactttttaa agcttttttg gagggtaaaa 11580 gtaatagtta cacaaaataa aaatacaaat ggtacaaaag gacttagaat ggaaacatgt 11640 ttctctcccg actccagcct cctgtttttc ttcccagaga ctgaccactg ctgtctgtct 11700 cttgccagaa gggaaaggga ggcaaggtta gggcaggcag agggcatgtg catcctttag 11760 agagagctta tgtctataca agcaaatgtg tgtgttcagt catcgctgtc ttagttttct 11820 attgctgcat aataatggta ctaccagctt cacagcttta aacaacaccc atttattatc 11880 tcatagtttc tgtggttggg agtctggaca tagcttagcc aggttctctg ctttagagtc 11940 tcgtgaggct ataatcaagg tgtgggatgg ggctgcagtt tcatctgagg ctcaattggg 12000 gaagggtcac ttctaagctc atacaatatt ggtgacattc agtccctggc aggctgttga 12060 actgagagcc tcagtttcgt gctggctgtt ggttgtagtt aaccctgaat tccttcccat 12120 gtgccctttg caaagccatc aaggcagaga gacttgccta gcaagtagga tattacagtc 12180 ttctgtaata taatcacatc catgaaatcc tctatatatc ccatcacctt taccatattc 12240 tgtgggttag aaacaagtag caggtcctgc ccacactcga gaagaccaga tgacacaaag 12300 atgtgattca aagtggggat catcggggcc atcttaggtt tgtctgcagt gatcactgtg 12360 ccatctctct ctctctcttt tttttttttt tttttccgag acgaagtcgt cactctgtca 12420 cccaggctgg agtgcagtgg catgatctca gcttaccaca atctctgcct cccaggttca 12480 aatgattctt ctgcctcagc ctcctgagta gctgggatta caggtgcccg ccaccacacc 12540 cagctaattt ttgtattttt agtagagaca gagtttcacc atgttggcca ggctggtctt 12600 gaactcctca cctcaagtga tccacccact tcggcctccc aaagtgctgg gattacaggc 12660 atgagccacc atgcccagcc ccatctctct ttaaaaaaca aacaaacaaa caaaaaacat 12720 aaaaagaagc agagaacaca tacacatctg catcttccct tgtttactta acaatagatc 12780 ttggaagtca cttctcagta gaggctaggt tgggcagagc attggattct aggccagtga 12840 gtttggactt gaccatggag acactaggaa gcccatgaag gacagagaga gatgcctcga 12900 ccctgccagt cctttagaaa gatcacccag tgctttttgt ataccaaacc ctatttgaaa 12960 tacttacgta tattaaccca tttccttatc accacaaccc tgcgggaagg gagataggca 13020 cttttattat cttcattttg cagatgagga cattgaggtc cagagaggtt atgtcactta 13080 cttaaggtca cacagccagg aagtggtagt agggactctt acccttgttt tacagatgag 13140 attgaattat ctcacgaaaa ctcagaaagg ttaaacaact tgcctaagta acatacagct 13200 aattagtcga ggagcctgac gcatgttgct ctagcctggt cacagttaca gaggtggcaa 13260 gcaatggcct gaacaggacg aacaaccaaa tacccaggct ggtggctctt aaacatggtg 13320 gggtcagcta acgacagcaa ccagggtggg cactggtgcc cctcgccccc ggctggtgcc 13380 ctaacatctc ccttttctct accagttcag aatctataac gtgacctacc tagaaccctc 13440 cctccgcatc gcagccagca ccctgaagtc tgggatttcc tacagggcac gggtgagggc 13500 ctgggctcag tgctataaca ccacctggag tgagtggagc cccagcacca agtggcacaa 13560 ctgtgagtat caagaggcct aagcaatggt aatctccact ctccattctt cccctgtggc 13620 cagacacttc ccctggctga gtctctgggc ttttatatca taggatgcct ctaatggcaa 13680 tcctgccatt agatacacct gctgtggtgt atctgccagg taggcaggct aggctgcagt 13740 aacacacaag cccacaattt ccatggctta acactatagg aatatatttc ttgctcatgt 13800 aacaagctaa cgtgaatgtt gctggtttgt aggtggtttc cctccctgta gaaatctggg 13860 gagtgaggtt ctttccatct tgtggtgcca tcattctcca ggacaaagat tcttacctac 13920 ttttgtgtcc tggtttcctt tggcagcctg gtgaagccta tggacctcat ttcagaatat 13980 ttttaaatac ataaaatccc agcctgggca atatagtgaa acccccatct gtacaaaaat 14040 tagccaggca tggtggcatg cacctgtagt cccaggtact gggaaggctg aggtgggagg 14100 atcacttgag cccaggagtt tgaggctgca gtgagccgtg atcgtaccac tttactccca 14160 cctgggtgac agagcaagag cccatctcta aaaataaata aatacaatga aataaaataa 14220 aataaataga actacagagg aaactaattg tattgaaatg cagttataaa acatttaaac 14280 acatttttaa tctagagata tatgtgcttc tttattaaga tctataaata ataagttcta 14340 ggggtagctc gcataaatac tgtaatttca aagtagataa gcataaataa tactttatga 14400 tactgaaatt gtgatgtgat atgagaatag ctgtgagttt tgttttgctg gggacaggat 14460 cactgatgct gtcattactg gggtctcttc cctccattct ttttttaaaa ttgtatttta 14520 ttttattttt aaaattttaa aataaataga gacagggtat cactatgttg cccaggctgc 14580 ttttgacctc ctgggctcca gtgatcttcc catcttggct tcccaaagtg ctgggattac 14640 aagtgggagc cagtgttcct ggccccttcc tccattctta atggaaggag atgctaggtg 14700 tgagaggtta gggaaagtaa agatgtaatt tctttcccat ccaagttctc agacccctga 14760 attctacctg cagccatgtt ggtccatcaa ccccaagtga agaatccctg ctctagggcc 14820 ccaccattgt ctgtatccag ccagcagaag aggcgtgatt atggagatca catctgcttc 14880 ttgaaagcag acagcccgga agtgggccgc atcacttcct ctcaaattct attggtgaaa 14940 atggtcacat gactacacat agccacaaag gaggctggga actttctcac ttggaaccta 15000 catcccagaa acaactcttt tcagtgaggt atcccacagg tctttcgcag tagaaatatt 15060 gattatctca cataaaatga agtcttacaa atggacctac tgggttttgt acagcagcca 15120 agtgatatct cttcccttct gctgtcttcc cttctgccgt ccttcacatg gtggcattgt 15180 atccttagac ttgccaccca tgccctcagg ttggccgttg cacactgtct tacataaagc 15240 aggaaggaaa ggaaaggctg ctacgagaga gtgtaccttg tgcatctctt ttttaatcag 15300 gaagcaaaca tctttctaga agcttcccta gcaaaattcc ccttacatct cattggccaa 15360 gactgttaca tgttacatgg ttactgttat tacttgctca ttgcaaggaa gactgggaac 15420 tcaaatgcct ggaaaaagga acaggataat cgtgattggc tcaagcctta gggtgggcat 15480 ggctccctga caagggagag aggaaaaagc tgttgagtga agaagactgc ttcagtttcc 15540 ccatctgtat aatgggagga gtaagggctg tcgtgaaaac tcaatgaaag aagattcttc 15600 aacgtggtag gtgcagtggc agctggcagt accctgaccc tgccaccgca cagccctctc 15660 agcattgctc atcctgcact gtggatatca gttgagccac gtgtctcctg ccctgggctg 15720 tgagctccat aggcagggtc tccatggctg tatctccaga acccagcaca gaaccaggtg 15780 cttgggaaag ttttgaattg attctcatct gccattggca tggggaaggg aactagcttg 15840 tatgaaacag ataacaatgt atgggaccct cattcattat ttcagcaaat atttgctgag 15900 ttcctcctac atggctagcc ctgtgctaga cactggggaa tcggcgatga acaaagcaga 15960 tagaaatccc cactcttgtg gagctgacat tctggaggga gagacaaaaa gcaaacatat 16020 aaagaaagaa agaaatcaca tggatctgga tgacagtgag tgctgggaag aaaataaaag 16080 cagaggaagg ggatggagcg atgggcaggg ggcaacggta gggagggtgt cggggaaaac 16140 tttttggaga atgtgacgat gaaagtgaac aaggagaagt caaccgtgtt gagatgatgg 16200 cagctaatga tgtggacagg ccactctgtt ctgagtgcat tatctattga ttcatcatgt 16260 catcctcgca acagccctgc acgatcaatt ctgtcattaa ccccatagta cagatgagga 16320 tgcggaggca cagagaagat aagggacttg tcctgtgtca cacagcaagg agccatccgg 16380 ctcctaagtt ggtgcatttg acttctgtgc ttccggaaag aaagagcagc aagtttaaga 16440 tctggaggtg gcactgagct ttggaggagc agggggcaat gaggtggccg gtgtgacgag 16500 gactcaatgt gcaagaggga gagtggtggg gagatgaggt ggaggggtgg tcggcggtca 16560 gatcgtggag ggtctcggac gagggtcctg accctgggtc tccagtcctg ggaagtggag 16620 cccaggctgt accatggctg acctcagctc atggcttccc ctcccacttc cagcctacag 16680 ggagcccttc gagcagcacc tcctgctggg cgtcagcgtt tcctgcattg tcatcctggc 16740 cgtctgcctg ttgtgctatg tcagcatcac caagtgagtc ctgggcccag tgctgccgag 16800 cagtccctct ggagtgcagg gtggcaggga cttgcccctc tagtctgccc ctttgcagtc 16860 ctctcagtca ataatacgta tttactgagc agctactaca caccttgaga gtagagctga 16920 gaacatatcg acaaggaccc cacttttttc tttttttctt tttttttttt ttttgagacg 16980 gagtctcact ctgtcaccca ggctggagta tagtggcaca atcttgccta acagtaacct 17040 ccgcctcccg ggttcaagca attcttctgc ctcagcctcc agagtagctg ggattacagg 17100 cgcatgccac tatgcccggc taattttttg tatttttggt agagatgggg tttcaccatg 17160 ttggtcaggc tggtctcgaa ctcctgacct catgatctgc ctgcctcagc ctcccaaagt 17220 gctgggatta caggtgtgag ccactgcacc caaccaggac tccacatttc taaaaccggc 17280 atcctactgg ggagactgaa aatacatatc aatcacaaac aggtggtttt ccatagtgac 17340 ccactctctg aatgcactag accagggtgg aggccagaga tcttctgggg tgctttttgc 17400 aagggggacc aggataaggc tctccaagga gggaaaattt gaggggggcc ctgactgggg 17460 agaatgagct ggccagggat aagcaagatg gagtcatccc acatcccctt acaacactgg 17520 gtgcctgggc aactgggggc atttgggggc atgtggtagg agccagagga atttgcgacg 17580 attgccctga tggagtcagg agacctgggt ttgaatcctg gccttggagc ttggtagctg 17640 gcggccgaca agttgctgaa acccctgagc ctggggttcc tgctttgcag agtgacagtg 17700 atggtgagaa catatttcat cagccagaag aggccaaatc acagtaaagg ctgagggagg 17760 agatgagtgg cgagtggctg ggaggtggtg gaaggagcct cgtttccaga gagctcttgc 17820 cagcccttgg aatcatggtg tctcagagcc tcagtcctcc catctctgaa atgggactag 17880 caagctcaac ctcactaagt caggattaga ggtggctaag gattattaac atgattgatg 17940 aaagtgccca ctcttggccc agcacacact aggtaggcag ggaatgcaaa ttcccctcca 18000 tatcttgtca ctgatgcctc cgagcaacct tggactgatc gccttgctct gagcctcagt 18060 ttccccatca cctgtacctc ttcccactcc ccatcactat atcccagcat gccagcctct 18120 ttgctgttct ttgtctttgg tttcttgttt tgttctgttt tttagacagg gtctcactct 18180 gttagccagg ctgaagtgca gtggcgcggt tacggctcac tgcagcctcc aattcctggg 18240 ctaaagagat cctcccattt caacttccag agcagctggg acaacaggcg cttgccacca 18300 cacctggcta attttcttat tttaatttaa ttttatttta ttttttggga cagagtggag 18360 tctcaaaaac caagctagag tgcagtggtg cgatctcgac tcactgcaat ctctgcctcc 18420 cgggttcaag cgattctcct gccttagcct cccgactagc tgggattaca ggcgtgtgcc 18480 acgacaccca gctaattttt gtatttttag tagagatggg gtttcaccat gttggccagg 18540 atggtcttga actcctgacc tcaagtgatc cacccacctc gttctcccaa ggtgctgggt 18600 acaggcatga gccactgtgc ctggccaatt ttcttacatt ttgtagagac tggctgtcac 18660 ttatgtagcc caggctgatc ttgaacttct acccctttat ctttattcat ggcacttatt 18720 accatgaatg aatgacctca tataagcatt tctttcgttt tttttttttt ttctttgaga 18780 tggagtctca tgttgtcccc caggctggag tgcagtggcg cgatctcagc tcactgcaac 18840 ctccgccttc cgggttcaag cgattctcct gcctcagcct cctgagtagc tgggattgca 18900 ggcgcctgcc accatgcctg gctaagtttt gcatttttag tagagacggt gtttcaccat 18960 attggccagg ctggtctcga acttctgacc tcaggtgata cacctgcctt ggcctcccaa 19020 agtgctggga ttacaggcgt gagccgccat gcctggcctc atataagcat ttctgtctcc 19080 atttatcatc catctttccc tcttgaaggt cagtttcacc aaggcaggca tctttgtctc 19140 gttcactgtt gtagcctcag ggccaggcac agtgagtcaa acatagaagg tgctcaataa 19200 atatgtgttt atttattgaa accatgggca gaggctaatt cagaagcggt ctgaggacct 19260 tacctcccag tgatgatgca ccatggcccc aggcaggcca ggaagagaga agggttgtgt 19320 ttctccgtag gtcccccagc ttcccaggcc atcccaggcc attccctggt catttgccct 19380 cagctgctct gaaaaaggga ttgttgaggg gaacctagaa tcctctctct gcagtttgag 19440 tctttcctaa tcccctgggg tctcattccc actgaggaca taggtggcct cctcaggaac 19500 tctgtgctgg gtaacagaat gcgggagtgt gaacctggct ctgccaccta ccagctgtca 19560 ctccacctcc ttgggcctca ctctcctcat ctgtagaata gggttagcaa tagaatccat 19620 gtcaccaggt tagaatgatg agtcagtggt ttgacctcca gaaactaatc agcctgatct 19680 ctgatgccaa ataagtattg gtgataacga ccacttttat gggaggagcg ttcacctgtc 19740 aataattcag agatcaacac cttttccttt tgtttttcag gattaagaaa gaatggtggg 19800 atcagattcc caacccagcc cgcagccgcc tcgtggctat aataatccag gatgctcagg 19860 taggagtagg cgtggatgag gacatgtggg actgtgtaca tgaagaagtg tggttcagaa 19920 cacctgggct gttaaggacc ttcactggct tctggaatgg caaatagaca gtcaggaggg 19980 ttgcagggga gacagaggca gaagccgaat gaggtcatta gcagaccaga ggctttcccg 20040 cccttcccct tggcaatccc agcctggggt gggcttctct ggggttggtt tcctgttttt 20100 ttccctcccc ttgggagaat gacccttggg tcatcatcac tgtgtcattc cctggggagg 20160 tgccagtacc agggctagag gccagaagga gtggaggaag gagagggtga caggctttct 20220 gtgtcttctt cttaagcata ggaaactgcc cccgaagcac tagcaaatcc cttccgggtt 20280 ctcattggcc tgaaatgtat cccaccccta agccaggggt ggagtcagct tccccaaggc 20340 gatggtcctg tgggtgagtg ggtggggttt gcctgagcaa gatgagagtt ctctaggtag 20400 gagaaagggg gattataggt cctgtctaga agagaaggtc tgagggtcct tgcttttcca 20460 gggactctgg aatctagtgt tggctttgaa tcctgactct gccactcact ggcagtgtgg 20520 acttgagcaa gttgcttaat tctctgagcc tcagtttcct cttgtgggtt ataacagtgt 20580 ttacctggta ggacagatat tggaatttat tgagacaata catataaagt gcatattcca 20640 gcctcttgca aataccaagt gccatttatg tatcagttag tgtttgctgt gtaacaaatg 20700 accccgaaat gtagagggtt acaacaactt tatttagctt atgcttctgc aggctggcat 20760 ttggggctgg gctcagcagt gagggtggcg ggggaggctg ggctgggctg ggctgggcag 20820 atctgaattg agctgacccg tccccgtagc ctccctccgt gtctgacagt tggctttttt 20880 tttttttttc tttttctgag acggagtttt gctcttattg cccaggagtg caatggcatg 20940 atcttggctc actgcaacct ctgcctcctg ggttcaagca attttcttgc ctcagcctcc 21000 caagtagctg ggattacagg catgtgccac cacgccaggc taattttgta tttttaatag 21060 agatggggtt tcttcatgtt ggtcaggctg gtctggaact cctaatatca gatgatccac 21120 ccacctcagc ctcccaaagt gctgggatta caggcgtgag ccactgcacc cagcctagtt 21180 ggctgacttt tacctgggac agtgcaggtg cctgagccat gtgcctctca ctctccagca 21240 ggccggccca ggcttgttta cagagtggct cagttttcaa gggtgggaag tcccaaggct 21300 tcttgaggcc taggcgcagc actggcatga tatcacttcc atcacattct atgggcccaa 21360 gcaagtccca gggccagtgt agattcaagg gatgggagga gattcagagc actcctctgt 21420 ggccactttt gccatcgacc acagtccctg taaatattag gacaatgtaa ttaattccca 21480 ggaatctgag gctcagaaag cgtaagtgac ctgttggact tctgatctgt gtgatgtcga 21540 ggcttgtacc ccttcctgag cattgccgta ctccaggccg ggctgcaagg ccactctgct 21600 ctttcattgg ctgtctctgt attttagggg tcacagtggg agaagcggtc ccgaggccag 21660 gaaccagcca agtgcccgta tgtatctgaa cttaggtcac agcctgcatg cattgggaag 21720 gtgatagaat tggagaggca agcccctagc tccatgtctg ccttctcttc cctgcattcg 21780 gtaattgccc tgtgacatta gccttcaagg gacggcagga ggaggggtgt tctggaaacg 21840 tggactgctg gccaagcccc ctgagtttca ctggtgtgtc aggtacatgg tgatacccct 21900 tgggagtgct gttatagtta acaaccagag cagccgtgcc tgttgttaaa atcttgacct 21960 aattgtatac ttgtcggcaa atagccacta tcctgaacac tcccctcctt ttttttaata 22020 tacaggatct cactctgtgg cccaggctgg tgtgcagtgg tgcgatcata gctcactgca 22080 ccttcaaact cctgagctca agtgatcctc ccatcttagc ctcccgagta gctgatacta 22140 cagatgtgca ttaccacgcc tggctatttt aaaaggtttt tgcctgtaat tccagctact 22200 caggaggctg aggcatgaga atcacttgaa cccgggaggc agaggttgca gtgagcgcag 22260 attgtgccac tgcactccag cctgggcgac agagtgagac tcttgtctca aaaaaaataa 22320 taccaaaaaa agtttttgta aagacaagct ctcgctgtgt tgccccgcca ctgtggcctc 22380 cttagcttct tccctggggc ctgctggacc tttccatact ccagaaacta aagggggtcc 22440 aggaccctgc ttcaacccta ggatcccgca tctttttttt tttttttttt ttttggacgc 22500 agggtcttgc tgtgtccctc aggctggagt gcagtgattc actgcagcct caaactcgtg 22560 ggctcaagtg attctctagc ctcagccttc taagtagctg ggactacagt catacaccaa 22620 catgcccagc taattttcct tttttttaat tcttgtagag atgtttgaga cggcttgggc 22680 tctgttgccc aggctgttct caaactcctg agctcaagcg atcctccctc ctcagcctcc 22740 taaagtgctg ggattacagg cgtgagccac cgcacccggc ttccatatcc tttctaattg 22800 gtcatggctt gggataatgg tgttgctttt aattatcatc atccataaag actttttctt 22860 actcaacaga tctgagcttg tatttggtgc ccaggacatg tgctgggttc ccgaaatccc 22920 aaagacacag accctaccct cagggatttc tcattctagc aacatagact gatcaattac 22980 tgattataac gttagaaggc atgtctgaag tagacagcca tcaggacatg gtgatttcag 23040 gctgggcttt gaagaatgaa taggagtttt tcaagtgtcg aaactgaacc ctgaccaacc 23100 tttgcttttg cagacactgg aagaattgtc ttaccaagct cttgccctgt tttctggagc 23160 acaacatgaa aagggatgaa gatcctcaca aggctgccaa agagatgcct ttccagggct 23220 ctggaaaatc agcatggtgc ccagtggaga tcagcaagac agtcctctgg ccagagagca 23280 tcagcgtggt gcgatgtgtg gagttgtttg aggccccggt ggagtgtgag gaggaggagg 23340 aggtagagga agaaaaaggg agcttctgtg catcgcctga gagcagcagg gatgacttcc 23400 aggagggaag ggagggcatt gtggcccggc taacagagag cctgttcctg gacctgctcg 23460 gagaggagaa tgggggcttt tgccagcagg acatggggga gtcatgcctt cttccacctt 23520 cgggaagtac gagtgctcac atgccctggg atgagttccc aagtgcaggg cccaaggagg 23580 cacctccctg gggcaaggag cagcctctcc acctggagcc aagtcctcct gccagcccga 23640 cccagagtcc agacaacctg acttgcacag agacgcccct cgtcatcgca ggcaaccctg 23700 cttaccgcag cttcagcaac tccctgagcc agtcaccgtg tcccagagag ctgggtccag 23760 acccactgct ggccagacac ctggaggaag tagaacccga gatgccctgt gtcccccagc 23820 tctctgagcc aaccactgtg ccccaacctg agccagaaac ctgggagcag atcctccgcc 23880 gaaatgtcct ccagcatggg gcagctgcag cccccgtctc ggcccccacc agtggctatc 23940 aggagtttgt acatgcggtg gagcagggtg gcacccaggc cagtgcggtg gtgggcttgg 24000 gtcccccagg agaggctggt tacaaggcct tctcaagcct gcttgccagc agtgctgtgt 24060 ccccagagaa atgtgggttt ggggctagca gtggggaaga ggggtataag cctttccaag 24120 acctcattcc tggctgccct ggggaccctg ccccagtccc tgtccccttg ttcacctttg 24180 gactggacag ggagccacct cgcagtccgc agagctcaca tctcccaagc agctccccag 24240 agcacctggg tctggagccg ggggaaaagg tagaggacat gccaaagccc ccacttcccc 24300 aggagcaggc cacagacccc cttgtggaca gcctgggcag tggcattgtc tactcagccc 24360 ttacctgcca cctgtgcggc cacctgaaac agtgtcatgg ccaggaggat ggtggccaga 24420 cccctgtcat ggccagtcct tgctgtggct gctgctgtgg agacaggtcc tcgcccccta 24480 caacccccct gagggcccca gacccctctc caggtggggt tccactggag gccagtctgt 24540 gtccggcctc cctggcaccc tcgggcatct cagagaagag taaatcctca tcatccttcc 24600 atcctgcccc tggcaatgct cagagctcaa gccagacccc caaaatcgtg aactttgtct 24660 ccgtgggacc cacatacatg agggtctctt aggtgcatgt cctcttgttg ctgagtctgc 24720 agatgaggac tagggcttat ccatgcctgg gaaatgccac ctcctggaag gcagccaggc 24780 tggcagattt ccaaaagact tgaagaacca tggtatgaag gtgattggcc ccactgacgt 24840 tggcctaaca ctgggctgca gagactggac cccgcccagc attgggctgg gctcgccaca 24900 tcccatgaga gtagagggca ctgggtcgcc gtgccccacg gcaggcccct gcaggaaaac 24960 tgaggccctt gggcacctcg acttgtgaac gagttgttgg ctgctccctc cacagcttct 25020 gcagcagact gtccctgttg taactgccca aggcatgttt tgcccaccag atcatggccc 25080 acatggaggc ccacctgcct ctgtctcact gaactagaag ccgagcctag aaactaacac 25140 agccatcaag ggaatgactt gggcggcctt gggaaatcga tgagaaattg aacttcaggg 25200 agggtggtca ttgcctagag gtgctcattc atttaacaga gcttccttag gttgatgctg 25260 gaggcagaat cccggctgtc aaggggtgtt cagttaaggg gagcaacaga ggacatgaaa 25320 aattgctgtg actaaagcag ggacaatttg ctgccaaaca cccatgccca gctgtatggc 25380 tgggggctcc tcgtatgcat ggaaccccca gaataaatat gctcagccac cctgtgggcc 25440 gggcaatcca gacagcaggc ataaggcacc agttaccctg catgttggcc cagacctcag 25500 gtgctaggga aggcgggaac cttgggttga gtaatgctcg tctgtgtgtt ttagtttcat 25560 cacctgttat ctgtgtttgc tgaggagagt ggaacagaag gggtggagtt ttgtataaat 25620 aaagtttctt tgtctcttta ttttttatgt attaaccaaa catacctcca gacactgctg 25680 tgagtgctgt gtctctgtta actcctggaa ttcacccatc cagaggaacc aggatgcaag 25740 aggttaagaa acttgccgtc tgggtttggg ttccccatac aaggattcaa atagttgatt 25800 taggaagtaa tcccgggaaa ccctgctaag gtagtgggga actgaggcag ggaaggacac 25860 aaaccaagaa agtgttacct gaaaggggtc cagatgcaga ccccaaaaga gggttcttga 25920 atctcatgca agaaagaatt cagagcgagt ccatagagtc agtgaaagca agttaatgag 25980 gaaagtaaag gaataaaaga atggctactc cgtagacaga gcagccctga gggttgctgg 26040 ctgcctattt ttatggttat tgattaatta tattccaaac aaggggtgga ttattatgcc 26100 tcccttttag accatatagg gtaacttcct gatgttgcca tggcatttgt aaactgtcat 26160 ggcgctgttg ggagtgtagc agtgaggaca accagaggtc actcttgttg ccatcttggt 26220 tttggtgggt tagagccatc ttctttactg caacctgttt tatcagcaag gtctttatga 26280 cttgtatcgg tgacgacctc ctgtctcatt ctatgactaa gaatgcccta acctcccagg 26340 aatgcagccc agtaagtctc agcctcattt tacccagccc ctcttcaaag ctccagttta 26400 aataaacctc tgacaaaagg gtgagttatt caacagatta ccagcatgag taactgatgc 26460 ttacctgccg gggatctctg gaagaccatg catggcacat gcccagttat gcctgcaaag 26520 gagagggagc tggggtattt gtccaccagc tcccatctgt cattggctga gagctgcttc 26580 caggagcatt aattctccag cacttccagc tactccagga aaaaaaaaat tcttcaactg 26640 agagttggag gtgttgagag actctggcac accaagaaga caggaacagg acaccaacag 26700 tggctgatga tacactgcca aggtcacaca gctagttagc aacagatcta tagtggaatc 26760 cagacagtgt ctccatcacc caggctctct gtagtgatct gcgcttcaca tccgaggcag 26820 gcagagggat ggtgtgggcc ttagatggga aggctgggaa cctgaagctc ctatgtctgt 26880 atcacttttg cttctctgag tagctgccct gatttcacac ttgaggggct tggccatttt 26940 agattccttc ctgctctagg agcctacata ctacactgga aatgatgggg agctctctac 27000 ctcacatgca gcctgatgtt tgttagaaac acctccttgc gccaggcatg atggctcatg 27060 gctgtaatcc cagcaatttg ggaggctgag gcgggtgtat cacttgaggt gaggagttca 27120 agaccagcct ggccaatatg gtgaaaccct atctctacca aaaaataaaa aattagccgg 27180 gtgtggtggt gggtgcctgt aatctcagct acttgggagg ctgagttggt agaattgctt 27240 caacctggga cgcggaggtt gcagtgagct gagattgtgc cattgcactc cagcttggat 27300 gacagagtga gaccctgtct caggaaaaaa aaaaaaaaac aaaaaaaacc ttgttctaag 27360 ccaaaatcaa tccctttagc tgcccaaatc acacagttta cagatggaga aacagtttta 27420 gagaggaaaa gggacttgcc caaagtcacc cagagaatgg cagagcctga actagccttc 27480 tggacttctt gcctccaaaa gctctttata ataaaatata attttaaata aaaatagtta 27540 tctgtttagg gccaagcaat atgctaagtg ccgtccagcc actgtgtcat ttacgtctcc 27600 aaacagctct agttgggagg ctcaatgatt atcccaattt tacagataag gaaacaggtc 27660 cagagaggtt gaggattagc ctagaaccac acagctagga aatcctggag ccaggatttg 27720 aacccgggtc tgacctaaga gctcccagcc gccgtgatat atcagcttat gtcatcctga 27780 cacctacgca gatgtcggct cgaatccact ttgcctgagc attgtctcag agaaatctaa 27840 tttaaaaatt aggcagcaaa tagaaaatat atttgactgc tagagatgca atgggactgg 27900 gagcccaaca aaggatctta ggcaaaagaa atccaagttg ttggcctcag caactattac 27960 tgaactggct gggctttggg aagctacaga gggatgagaa gacctggtgg atcaggtggg 28020 cccaactcag gctggccccc accctgcagg aagtaggaaa agtccagggt cataggccca 28080 gtgagatgcc ggctgcggga gtttcagcct ccggggctgg accagagggc aggaggggac 28140 gcccctgggt agcagcgcca gagtgggctg agtggcctgg gcccctgcgg gggagctttc 28200 agagatgttg atttgggggt actccctcag ccctgccttt acacagaatt tgtgggggat 28260 gaggggaggg ggaaaggggg gaggaaggca gtgagtgcat ctgaattttt tttttttttt 28320 tacaaaaagt ggcttattgc atttttctga ttactctatc agcacgtgca gaccttttcc 28380 tattcagaga aagcctgaag atataaagag gaaagtgaag aaaaaccacc ggaaatccca 28440 tccccgcccc agcatctggc actgtgtggg cgatcacgaa atgagcgctt gtttttgaag 28500 gcgtagtatc tccgtgaaca tccggttgaa caacctttct gactttattt ttcccacgaa 28560 agttattaat taaaaaacaa aaagcaaaac accgaaaaaa caaaaaaccc agcaagtgtt 28620 tgagctccca ccacgaggga ggcctgacgt cactggatcc tcccggcagc cgatgaggct 28680 gcatgggact 28690 2 2476 DNA Homo sapiens 2 atggggtggc tttgctctgg gctcctgttc cctgtgagct gcctggtcct gctgcaggtg 60 gcaagctctg ggaacatgaa ggtcttgcag gagcccacct gcgtctccga ctacatgagc 120 atctctactt gcgagtggaa gatgaatggt cccaccaatt gcagcaccga gctccgcctg 180 ttgtaccagc tggtttttct gctctccgaa gcccacacgt gtatccctga gaacaacgga 240 ggcgcggggt gcgtgtgcca cctgctcatg gatgacgtgg tcagtgcgga taactataca 300 ctggacctgt gggctgggca gcagctgctg tggaagggct ccttcaagcc cagcgagcat 360 gtgaaaccca gggccccagg aaacctgaca gttcacacca atgtctccga cactctgctg 420 ctgacctgga gcaacccgta tccccctgac aattacctgt ataatcatct cacctatgca 480 gtcaacattt ggagtgaaaa cgacccggca gatttcagaa tctataacgt gacctaccta 540 gaaccctccc tccgcatcgc agccagcacc ctgaagtctg ggatttccta cagggcacgg 600 gtgagggcct gggctcagtg ctataacacc acctggagtg agtggagccc cagcaccaag 660 tggcacaact cctacaggga gcccttcgag cagcacctcc tgctgggcgt cagcgtttcc 720 tgcattgtca tcctggccgt ctgcctgttg tgctatgtca gcatcaccaa gattaagaaa 780 gaatggtggg atcagattcc caacccagcc cgcagccgcc tcgtggctat aataatccag 840 gatgctcagg ggtcacagtg ggagaagcgg tcccgaggcc aggaaccagc caagtgccca 900 cactggaaga attgtcttac caagctcttg ccctgttttc tggagcacaa catgaaaagg 960 gatgaagatc ctcacaaggc tgccaaagag atgcctttcc agggctctgg aaaatcagca 1020 tggtgcccag tggagatcag caagacagtc ctctggccag agagcatcag cgtggtgcga 1080 tgtgtggagt tgtttgaggc cccggtggag tgtgaggagg aggaggaggt agaggaagaa 1140 aaagggagct tctgtgcatc gcctgagagc agcagggatg acttccagga gggaagggag 1200 ggcattgtgg cccggctaac agagagcctg ttcctggacc tgctcggaga ggagaatggg 1260 ggcttttgcc agcaggacat gggggagtca tgccttcttc caccttcggg aagtacgagt 1320 gctcacatgc cctgggatga gttcccaagt gcagggccca aggaggcacc tccctggggc 1380 aaggagcagc ctctccacct ggagccaagt cctcctgcca gcccgaccca gagtccagac 1440 aacctgactt gcacagagac gcccctcgtc atcgcaggca accctgctta ccgcagcttc 1500 agcaactccc tgagccagtc accgtgtccc agagagctgg gtccagaccc actgctggcc 1560 agacacctgg aggaagtaga acccgagatg ccctgtgtcc cccagctctc tgagccaacc 1620 actgtgcccc aacctgagcc agaaacctgg gagcagatcc tccgccgaaa tgtcctccag 1680 catggggcag ctgcagcccc cgtctcggcc cccaccagtg gctatcagga gtttgtacat 1740 gcggtggagc agggtggcac ccaggccagt gcggtggtgg gcttgggtcc cccaggagag 1800 gctggttaca aggccttctc aagcctgctt gccagcagtg ctgtgtcccc agagaaatgt 1860 gggtttgggg ctagcagtgg ggaagagggg tataagcctt tccaagacct cattcctggc 1920 tgccctgggg accctgcccc agtccctgtc cccttgttca cctttggact ggacagggag 1980 ccacctcgca gtccgcagag ctcacatctc ccaagcagct ccccagagca cctgggtctg 2040 gagccggggg aaaaggtaga ggacatgcca aagcccccac ttccccagga gcaggccaca 2100 gacccccttg tggacagcct gggcagtggc attgtctact cagcccttac ctgccacctg 2160 tgcggccacc tgaaacagtg tcatggccag gaggatggtg gccagacccc tgtcatggcc 2220 agtccttgct gtggctgctg ctgtggagac aggtcctcgc cccctacaac ccccctgagg 2280 gccccagacc cctctccagg tggggttcca ctggaggcca gtctgtgtcc ggcctccctg 2340 gcaccctcgg gcatctcaga gaagagtaaa tcctcatcat ccttccatcc tgcccctggc 2400 aatgctcaga gctcaagcca gacccccaaa atcgtgaact ttgtctccgt gggacccaca 2460 tacatgaggg tctctt 2476 3 825 PRT Homo sapiens 3 Met Gly Trp Leu Cys Ser Gly Leu Leu Phe Pro Val Ser Cys Leu Val 1 5 10 15 Leu Leu Gln Val Ala Ser Ser Gly Asn Met Lys Val Leu Gln Glu Pro 20 25 30 Thr Cys Val Ser Asp Tyr Met Ser Ile Ser Thr Cys Glu Trp Lys Met 35 40 45 Asn Gly Pro Thr Asn Cys Ser Thr Glu Leu Arg Leu Leu Tyr Gln Leu 50 55 60 Val Phe Leu Leu Ser Glu Ala His Thr Cys Ile Pro Glu Asn Asn Gly 65 70 75 80 Gly Ala Gly Cys Val Cys His Leu Leu Met Asp Asp Val Val Ser Ala 85 90 95 Asp Asn Tyr Thr Leu Asp Leu Trp Ala Gly Gln Gln Leu Leu Trp Lys 100 105 110 Gly Ser Phe Lys Pro Ser Glu His Val Lys Pro Arg Ala Pro Gly Asn 115 120 125 Leu Thr Val His Thr Asn Val Ser Asp Thr Leu Leu Leu Thr Trp Ser 130 135 140 Asn Pro Tyr Pro Pro Asp Asn Tyr Leu Tyr Asn His Leu Thr Tyr Ala 145 150 155 160 Val Asn Ile Trp Ser Glu Asn Asp Pro Ala Asp Phe Arg Ile Tyr Asn 165 170 175 Val Thr Tyr Leu Glu Pro Ser Leu Arg Ile Ala Ala Ser Thr Leu Lys 180 185 190 Ser Gly Ile Ser Tyr Arg Ala Arg Val Arg Ala Trp Ala Gln Cys Tyr 195 200 205 Asn Thr Thr Trp Ser Glu Trp Ser Pro Ser Thr Lys Trp His Asn Ser 210 215 220 Tyr Arg Glu Pro Phe Glu Gln His Leu Leu Leu Gly Val Ser Val Ser 225 230 235 240 Cys Ile Val Ile Leu Ala Val Cys Leu Leu Cys Tyr Val Ser Ile Thr 245 250 255 Lys Ile Lys Lys Glu Trp Trp Asp Gln Ile Pro Asn Pro Ala Arg Ser 260 265 270 Arg Leu Val Ala Ile Ile Ile Gln Asp Ala Gln Gly Ser Gln Trp Glu 275 280 285 Lys Arg Ser Arg Gly Gln Glu Pro Ala Lys Cys Pro His Trp Lys Asn 290 295 300 Cys Leu Thr Lys Leu Leu Pro Cys Phe Leu Glu His Asn Met Lys Arg 305 310 315 320 Asp Glu Asp Pro His Lys Ala Ala Lys Glu Met Pro Phe Gln Gly Ser 325 330 335 Gly Lys Ser Ala Trp Cys Pro Val Glu Ile Ser Lys Thr Val Leu Trp 340 345 350 Pro Glu Ser Ile Ser Val Val Arg Cys Val Glu Leu Phe Glu Ala Pro 355 360 365 Val Glu Cys Glu Glu Glu Glu Glu Val Glu Glu Glu Lys Gly Ser Phe 370 375 380 Cys Ala Ser Pro Glu Ser Ser Arg Asp Asp Phe Gln Glu Gly Arg Glu 385 390 395 400 Gly Ile Val Ala Arg Leu Thr Glu Ser Leu Phe Leu Asp Leu Leu Gly 405 410 415 Glu Glu Asn Gly Gly Phe Cys Gln Gln Asp Met Gly Glu Ser Cys Leu 420 425 430 Leu Pro Pro Ser Gly Ser Thr Ser Ala His Met Pro Trp Asp Glu Phe 435 440 445 Pro Ser Ala Gly Pro Lys Glu Ala Pro Pro Trp Gly Lys Glu Gln Pro 450 455 460 Leu His Leu Glu Pro Ser Pro Pro Ala Ser Pro Thr Gln Ser Pro Asp 465 470 475 480 Asn Leu Thr Cys Thr Glu Thr Pro Leu Val Ile Ala Gly Asn Pro Ala 485 490 495 Tyr Arg Ser Phe Ser Asn Ser Leu Ser Gln Ser Pro Cys Pro Arg Glu 500 505 510 Leu Gly Pro Asp Pro Leu Leu Ala Arg His Leu Glu Glu Val Glu Pro 515 520 525 Glu Met Pro Cys Val Pro Gln Leu Ser Glu Pro Thr Thr Val Pro Gln 530 535 540 Pro Glu Pro Glu Thr Trp Glu Gln Ile Leu Arg Arg Asn Val Leu Gln 545 550 555 560 His Gly Ala Ala Ala Ala Pro Val Ser Ala Pro Thr Ser Gly Tyr Gln 565 570 575 Glu Phe Val His Ala Val Glu Gln Gly Gly Thr Gln Ala Ser Ala Val 580 585 590 Val Gly Leu Gly Pro Pro Gly Glu Ala Gly Tyr Lys Ala Phe Ser Ser 595 600 605 Leu Leu Ala Ser Ser Ala Val Ser Pro Glu Lys Cys Gly Phe Gly Ala 610 615 620 Ser Ser Gly Glu Glu Gly Tyr Lys Pro Phe Gln Asp Leu Ile Pro Gly 625 630 635 640 Cys Pro Gly Asp Pro Ala Pro Val Pro Val Pro Leu Phe Thr Phe Gly 645 650 655 Leu Asp Arg Glu Pro Pro Arg Ser Pro Gln Ser Ser His Leu Pro Ser 660 665 670 Ser Ser Pro Glu His Leu Gly Leu Glu Pro Gly Glu Lys Val Glu Asp 675 680 685 Met Pro Lys Pro Pro Leu Pro Gln Glu Gln Ala Thr Asp Pro Leu Val 690 695 700 Asp Ser Leu Gly Ser Gly Ile Val Tyr Ser Ala Leu Thr Cys His Leu 705 710 715 720 Cys Gly His Leu Lys Gln Cys His Gly Gln Glu Asp Gly Gly Gln Thr 725 730 735 Pro Val Met Ala Ser Pro Cys Cys Gly Cys Cys Cys Gly Asp Arg Ser 740 745 750 Ser Pro Pro Thr Thr Pro Leu Arg Ala Pro Asp Pro Ser Pro Gly Gly 755 760 765 Val Pro Leu Glu Ala Ser Leu Cys Pro Ala Ser Leu Ala Pro Ser Gly 770 775 780 Ile Ser Glu Lys Ser Lys Ser Ser Ser Ser Phe His Pro Ala Pro Gly 785 790 795 800 Asn Ala Gln Ser Ser Ser Gln Thr Pro Lys Ile Val Asn Phe Val Ser 805 810 815 Val Gly Pro Thr Tyr Met Arg Val Ser 820 825 4 15 DNA Homo sapiens 4 ttgcaccact gcact 15 5 15 DNA Homo sapiens 5 ttgcaccgct gcact 15 6 15 DNA Homo sapiens 6 ttttgtgcta ttccc 15 7 15 DNA Homo sapiens 7 ttttgtgtta ttccc 15 8 15 DNA Homo sapiens 8 ctgggccgct caggc 15 9 15 DNA Homo sapiens 9 ctgggcctct caggc 15 10 15 DNA Homo sapiens 10 taagcctgcg ctgga 15 11 15 DNA Homo sapiens 11 taagcctccg ctgga 15 12 15 DNA Homo sapiens 12 agaacaacgg aggcg 15 13 15 DNA Homo sapiens 13 agaacaatgg aggcg 15 14 15 DNA Homo sapiens 14 cggaggcgcg gggtg 15 15 15 DNA Homo sapiens 15 cggaggcacg gggtg 15 16 15 DNA Homo sapiens 16 gtgcggataa ctata 15 17 15 DNA Homo sapiens 17 gtgcggacaa ctata 15 18 15 DNA Homo sapiens 18 cggagtgcgg caggg 15 19 15 DNA Homo sapiens 19 cggagtgtgg caggg 15 20 15 DNA Homo sapiens 20 gcctgggctg agggt 15 21 15 DNA Homo sapiens 21 gcctgggttg agggt 15 22 15 DNA Homo sapiens 22 tggggtgggc agggg 15 23 15 DNA Homo sapiens 23 tggggtgagc agggg 15 24 15 DNA Homo sapiens 24 ttctcccgca gtgaa 15 25 15 DNA Homo sapiens 25 ttctcccaca gtgaa 15 26 15 DNA Homo sapiens 26 gtgaaaacga cccgg 15 27 15 DNA Homo sapiens 27 gtgaaaatga cccgg 15 28 15 DNA Homo sapiens 28 ggcaagccct ggggc 15 29 15 DNA Homo sapiens 29 ggcaagctct ggggc 15 30 15 DNA Homo sapiens 30 gccctggggc tggat 15 31 15 DNA Homo sapiens 31 gccctggagc tggat 15 32 15 DNA Homo sapiens 32 atagcaaatc ccagg 15 33 15 DNA Homo sapiens 33 atagcaattc ccagg 15 34 15 DNA Homo sapiens 34 gctctgccct aggca 15 35 15 DNA Homo sapiens 35 gctctgcact aggca 15 36 15 DNA Homo sapiens 36 cccccacccc tcaca 15 37 15 DNA Homo sapiens 37 cccccactcc tcaca 15 38 15 DNA Homo sapiens 38 tccctccgca tcgca 15 39 15 DNA Homo sapiens 39 tccctccaca tcgca 15 40 15 DNA Homo sapiens 40 cacctgctgt ggtgt 15 41 15 DNA Homo sapiens 41 cacctgccgt ggtgt 15 42 15 DNA Homo sapiens 42 atgtctgaag tagac 15 43 15 DNA Homo sapiens 43 atgtctgcag tagac 15 44 15 DNA Homo sapiens 44 tgaccaacct ttgct 15 45 15 DNA Homo sapiens 45 tgaccaactt ttgct 15 46 15 DNA Homo sapiens 46 cctgttttct ggagc 15 47 15 DNA Homo sapiens 47 cctgtttcct ggagc 15 48 15 DNA Homo sapiens 48 tggacctgct cggag 15 49 15 DNA Homo sapiens 49 tggaccttct cggag 15 50 15 DNA Homo sapiens 50 agtcatgcct tcttc 15 51 15 DNA Homo sapiens 51 agtcatgtct tcttc 15 52 15 DNA Homo sapiens 52 gccttcttcc acctt 15 53 15 DNA Homo sapiens 53 gccttctccc acctt 15 54 15 DNA Homo sapiens 54 cagcccccgt ctcgg 15 55 15 DNA Homo sapiens 55 cagcccctgt ctcgg 15 56 15 DNA Homo sapiens 56 ggagtttgta catgc 15 57 15 DNA Homo sapiens 57 ggagtttata catgc 15 58 15 DNA Homo sapiens 58 cagctcccca gagca 15 59 15 DNA Homo sapiens 59 cagctcctca gagca 15 60 15 DNA Homo sapiens 60 agacaggtcc tcgcc 15 61 15 DNA Homo sapiens 61 agacagggcc tcgcc 15 62 15 DNA Homo sapiens 62 ctgcccctgg caatg 15 63 15 DNA Homo sapiens 63 ctgcccccgg caatg 15 64 15 DNA Homo sapiens 64 aggtgcatgt cctct 15 65 15 DNA Homo sapiens 65 aggtgcacgt cctct 15 66 15 DNA Homo sapiens 66 gtgcatgtcc tcttg 15 67 15 DNA Homo sapiens 67 gtgcatgccc tcttg 15 68 15 DNA Homo sapiens 68 ggcttatcca tgcct 15 69 15 DNA Homo sapiens 69 ggcttattca tgcct 15 70 15 DNA Homo sapiens 70 agccaggctg gcaga 15 71 15 DNA Homo sapiens 71 agccagggtg gcaga 15 72 15 DNA Homo sapiens 72 ggcccacatg gaggc 15 73 15 DNA Homo sapiens 73 ggcccacgtg gaggc 15 74 15 DNA Homo sapiens 74 taacacagcc atcaa 15 75 15 DNA Homo sapiens 75 taacacaacc atcaa 15 76 15 DNA Homo sapiens 76 taatgctcgt ctgtg 15 77 15 DNA Homo sapiens 77 taatgcttgt ctgtg 15 78 15 DNA Homo sapiens 78 acttgccgtc tgggt 15 79 15 DNA Homo sapiens 79 acttgccatc tgggt 15 80 15 DNA Homo sapiens 80 ctgagattgc accac 15 81 15 DNA Homo sapiens 81 ggctggagtg cagtg 15 82 15 DNA Homo sapiens 82 ctgagattgc accgc 15 83 15 DNA Homo sapiens 83 ggctggagtg cagcg 15 84 15 DNA Homo sapiens 84 ctgtgctttt gtgct 15 85 15 DNA Homo sapiens 85 accaagggga atagc 15 86 15 DNA Homo sapiens 86 ctgtgctttt gtgtt 15 87 15 DNA Homo sapiens 87 accaagggga ataac 15 88 15 DNA Homo sapiens 88 gagttcctgg gccgc 15 89 15 DNA Homo sapiens 89 ggagcagcct gagcg 15 90 15 DNA Homo sapiens 90 gagttcctgg gcctc 15 91 15 DNA Homo sapiens 91 ggagcagcct gagag 15 92 15 DNA Homo sapiens 92 tccgagtaag cctgc 15 93 15 DNA Homo sapiens 93 tccagctcca gcgca 15 94 15 DNA Homo sapiens 94 tccgagtaag cctcc 15 95 15 DNA Homo sapiens 95 tccagctcca gcgga 15 96 15 DNA Homo sapiens 96 tccctgagaa caacg 15 97 15 DNA Homo sapiens 97 accccgcgcc tccgt 15 98 15 DNA Homo sapiens 98 tccctgagaa caatg 15 99 15 DNA Homo sapiens 99 accccgcgcc tccat 15 100 15 DNA Homo sapiens 100 gaacaacgga ggcgc 15 101 15 DNA Homo sapiens 101 cacacgcacc ccgcg 15 102 15 DNA Homo sapiens 102 gaacaacgga ggcac 15 103 15 DNA Homo sapiens 103 cacacgcacc ccgtg 15 104 15 DNA Homo sapiens 104 tggtcagtgc ggata 15 105 15 DNA Homo sapiens 105 ccagtgtata gttat 15 106 15 DNA Homo sapiens 106 tggtcagtgc ggaca 15 107 15 DNA Homo sapiens 107 ccagtgtata gttgt 15 108 15 DNA Homo sapiens 108 gcagggcgga gtgcg 15 109 15 DNA Homo sapiens 109 agccacccct gccgc 15 110 15 DNA Homo sapiens 110 gcagggcgga gtgtg 15 111 15 DNA Homo sapiens 111 agccacccct gccac 15 112 15 DNA Homo sapiens 112 acagctgcct gggct 15 113 15 DNA Homo sapiens 113 caccccaccc tcagc 15 114 15 DNA Homo sapiens 114 acagctgcct gggtt 15 115 15 DNA Homo sapiens 115 caccccaccc tcaac 15 116 15 DNA Homo sapiens 116 tgagggtggg gtggg 15 117 15 DNA Homo sapiens 117 cctcctcccc tgccc 15 118 15 DNA Homo sapiens 118 tgagggtggg gtgag 15 119 15 DNA Homo sapiens 119 cctcctcccc tgctc 15 120 15 DNA Homo sapiens 120 ggccgcttct cccgc 15 121 15 DNA Homo sapiens 121 ctgggtttca ctgcg 15 122 15 DNA Homo sapiens 122 ggccgcttct cccac 15 123 15 DNA Homo sapiens 123 ctgggtttca ctgtg 15 124 15 DNA Homo sapiens 124 tttggagtga aaacg 15 125 15 DNA Homo sapiens 125 catctgccgg gtcgt 15 126 15 DNA Homo sapiens 126 tttggagtga aaatg 15 127 15 DNA Homo sapiens 127 catctgccgg gtcat 15 128 15 DNA Homo sapiens 128 ctgggaggca agccc 15 129 15 DNA Homo sapiens 129 tatccagccc caggg 15 130 15 DNA Homo sapiens 130 ctgggaggca agctc 15 131 15 DNA Homo sapiens 131 tatccagccc cagag 15 132 15 DNA Homo sapiens 132 aggcaagccc tgggg 15 133 15 DNA Homo sapiens 133 tttgctatcc agccc 15 134 15 DNA Homo sapiens 134 aggcaagccc tggag 15 135 15 DNA Homo sapiens 135 tttgctatcc agctc 15 136 15 DNA Homo sapiens 136 ggctggatag caaat 15 137 15 DNA Homo sapiens 137 ctagctcctg ggatt 15 138 15 DNA Homo sapiens 138 ggctggatag caatt 15 139 15 DNA Homo sapiens 139 ctagctcctg ggaat 15 140 15 DNA Homo sapiens 140 cacctggctc tgccc 15 141 15 DNA Homo sapiens 141 gggacttgcc taggg 15 142 15 DNA Homo sapiens 142 cacctggctc tgcac 15 143 15 DNA Homo sapiens 143 gggacttgcc tagtg 15 144 15 DNA Homo sapiens 144 cctggccccc caccc 15 145 15 DNA Homo sapiens 145 ctctgatgtg agggg 15 146 15 DNA Homo sapiens 146 cctggccccc cactc 15 147 15 DNA Homo sapiens 147 ctctgatgtg aggag 15 148 15 DNA Homo sapiens 148 gaaccctccc tccgc 15 149 15 DNA Homo sapiens 149 gctggctgcg atgcg 15 150 15 DNA Homo sapiens 150 gaaccctccc tccac 15 151 15 DNA Homo sapiens 151 gctggctgcg atgtg 15 152 15 DNA Homo sapiens 152 tagatacacc tgctg 15 153 15 DNA Homo sapiens 153 gcagatacac cacag 15 154 15 DNA Homo sapiens 154 tagatacacc tgccg 15 155 15 DNA Homo sapiens 155 gcagatacac cacgg 15 156 15 DNA Homo sapiens 156 gaaggcatgt ctgaa 15 157 15 DNA Homo sapiens 157 atggctgtct acttc 15 158 15 DNA Homo sapiens 158 gaaggcatgt ctgca 15 159 15 DNA Homo sapiens 159 atggctgtct actgc 15 160 15 DNA Homo sapiens 160 gaaccctgac caacc 15 161 15 DNA Homo sapiens 161 tgcaaaagca aagga 15 162 15 DNA Homo sapiens 162 gaaccctgac caatc 15 163 15 DNA Homo sapiens 163 tgcaaaagca aagaa 15 164 15 DNA Homo sapiens 164 tcttgccctg ttttc 15 165 15 DNA Homo sapiens 165 tgttgtgctc cagaa 15 166 15 DNA Homo sapiens 166 tcttgccctg tttcc 15 167 15 DNA Homo sapiens 167 tgttgtgctc cagga 15 168 15 DNA Homo sapiens 168 tgttcctgga cctgc 15 169 15 DNA Homo sapiens 169 tctcctctcc gagca 15 170 15 DNA Homo sapiens 170 tgttcctgga ccttc 15 171 15 DNA Homo sapiens 171 tctcctctcc gagaa 15 172 15 DNA Homo sapiens 172 tgggggagtc atgcc 15 173 15 DNA Homo sapiens 173 aaggtggaag aaggc 15 174 15 DNA Homo sapiens 174 tgggggagtc atgtc 15 175 15 DNA Homo sapiens 175 aaggtggaag aagac 15 176 15 DNA Homo sapiens 176 agtcatgcct tcttc 15 177 15 DNA Homo sapiens 177 ttcccgaagg tggaa 15 178 15 DNA Homo sapiens 178 agtcatgcct tctcc 15 179 15 DNA Homo sapiens 179 ttcccgaagg tggga 15 180 15 DNA Homo sapiens 180 cagctgcagc ccccg 15 181 15 DNA Homo sapiens 181 tgggggccga gacgg 15 182 15 DNA Homo sapiens 182 cagctgcagc ccctg 15 183 15 DNA Homo sapiens 183 tgggggccga gacag 15 184 15 DNA Homo sapiens 184 ctatcaggag tttgt 15 185 15 DNA Homo sapiens 185 tccaccgcat gtaca 15 186 15 DNA Homo sapiens 186 ctatcaggag tttat 15 187 15 DNA Homo sapiens 187 tccaccgcat gtata 15 188 15 DNA Homo sapiens 188 cccaagcagc tcccc 15 189 15 DNA Homo sapiens 189 cccaggtgct ctggg 15 190 15 DNA Homo sapiens 190 cccaagcagc tcctc 15 191 15 DNA Homo sapiens 191 cccaggtgct ctgag 15 192 15 DNA Homo sapiens 192 ctgtggagac aggtc 15 193 15 DNA Homo sapiens 193 gtagggggcg aggac 15 194 15 DNA Homo sapiens 194 ctgtggagac agggc 15 195 15 DNA Homo sapiens 195 gtagggggcg aggcc 15 196 15 DNA Homo sapiens 196 tccatcctgc ccctg 15 197 15 DNA Homo sapiens 197 tctgagcatt gccag 15 198 15 DNA Homo sapiens 198 tccatcctgc ccccg 15 199 15 DNA Homo sapiens 199 tctgagcatt gccgg 15 200 15 DNA Homo sapiens 200 tctcttaggt gcatg 15 201 15 DNA Homo sapiens 201 gcaacaagag gacat 15 202 15 DNA Homo sapiens 202 tctcttaggt gcacg 15 203 15 DNA Homo sapiens 203 gcaacaagag gacgt 15 204 15 DNA Homo sapiens 204 tcttaggtgc atgtc 15 205 15 DNA Homo sapiens 205 cagcaacaag aggac 15 206 15 DNA Homo sapiens 206 tcttaggtgc atgcc 15 207 15 DNA Homo sapiens 207 cagcaacaag agggc 15 208 15 DNA Homo sapiens 208 gactagggct tatcc 15 209 15 DNA Homo sapiens 209 tttcccaggc atgga 15 210 15 DNA Homo sapiens 210 gactagggct tattc 15 211 15 DNA Homo sapiens 211 tttcccaggc atgaa 15 212 15 DNA Homo sapiens 212 gaaggcagcc aggct 15 213 15 DNA Homo sapiens 213 tggaaatctg ccagc 15 214 15 DNA Homo sapiens 214 gaaggcagcc agggt 15 215 15 DNA Homo sapiens 215 tggaaatctg ccacc 15 216 15 DNA Homo sapiens 216 gatcatggcc cacat 15 217 15 DNA Homo sapiens 217 aggtgggcct ccatg 15 218 15 DNA Homo sapiens 218 gatcatggcc cacgt 15 219 15 DNA Homo sapiens 219 aggtgggcct ccacg 15 220 15 DNA Homo sapiens 220 agaaactaac acagc 15 221 15 DNA Homo sapiens 221 attcccttga tggct 15 222 15 DNA Homo sapiens 222 agaaactaac acaac 15 223 15 DNA Homo sapiens 223 attcccttga tggtt 15 224 15 DNA Homo sapiens 224 gttgagtaat gctcg 15 225 15 DNA Homo sapiens 225 aaaacacaca gacga 15 226 15 DNA Homo sapiens 226 gttgagtaat gcttg 15 227 15 DNA Homo sapiens 227 aaaacacaca gacaa 15 228 15 DNA Homo sapiens 228 taagaaactt gccgt 15 229 15 DNA Homo sapiens 229 acccaaaccc agacg 15 230 15 DNA Homo sapiens 230 taagaaactt gccat 15 231 15 DNA Homo sapiens 231 acccaaaccc agatg 15 232 10 DNA Homo sapiens 232 agattgcacc 10 233 10 DNA Homo sapiens 233 tggagtgcag 10 234 10 DNA Homo sapiens 234 tgcttttgtg 10 235 10 DNA Homo sapiens 235 aaggggaata 10 236 10 DNA Homo sapiens 236 ttcctgggcc 10 237 10 DNA Homo sapiens 237 gcagcctgag 10 238 10 DNA Homo sapiens 238 gagtaagcct 10 239 10 DNA Homo sapiens 239 agctccagcg 10 240 10 DNA Homo sapiens 240 ctgagaacaa 10 241 10 DNA Homo sapiens 241 ccgcgcctcc 10 242 10 DNA Homo sapiens 242 caacggaggc 10 243 10 DNA Homo sapiens 243 acgcaccccg 10 244 10 DNA Homo sapiens 244 tcagtgcgga 10 245 10 DNA Homo sapiens 245 gtgtatagtt 10 246 10 DNA Homo sapiens 246 gggcggagtg 10 247 10 DNA Homo sapiens 247 cacccctgcc 10 248 10 DNA Homo sapiens 248 gctgcctggg 10 249 10 DNA Homo sapiens 249 cccaccctca 10 250 10 DNA Homo sapiens 250 gggtggggtg 10 251 10 DNA Homo sapiens 251 cctcccctgc 10 252 10 DNA Homo sapiens 252 cgcttctccc 10 253 10 DNA Homo sapiens 253 ggtttcactg 10 254 10 DNA Homo sapiens 254 ggagtgaaaa 10 255 10 DNA Homo sapiens 255 ctgccgggtc 10 256 10 DNA Homo sapiens 256 ggaggcaagc 10 257 10 DNA Homo sapiens 257 ccagccccag 10 258 10 DNA Homo sapiens 258 caagccctgg 10 259 10 DNA Homo sapiens 259 gctatccagc 10 260 10 DNA Homo sapiens 260 tggatagcaa 10 261 10 DNA Homo sapiens 261 gctcctggga 10 262 10 DNA Homo sapiens 262 ctggctctgc 10 263 10 DNA Homo sapiens 263 acttgcctag 10 264 10 DNA Homo sapiens 264 ggccccccac 10 265 10 DNA Homo sapiens 265 tgatgtgagg 10 266 10 DNA Homo sapiens 266 ccctccctcc 10 267 10 DNA Homo sapiens 267 ggctgcgatg 10 268 10 DNA Homo sapiens 268 atacacctgc 10 269 10 DNA Homo sapiens 269 gatacaccac 10 270 10 DNA Homo sapiens 270 ggcatgtctg 10 271 10 DNA Homo sapiens 271 gctgtctact 10 272 10 DNA Homo sapiens 272 ccctgaccaa 10 273 10 DNA Homo sapiens 273 aaaagcaaag 10 274 10 DNA Homo sapiens 274 tgccctgttt 10 275 10 DNA Homo sapiens 275 tgtgctccag 10 276 10 DNA Homo sapiens 276 tcctggacct 10 277 10 DNA Homo sapiens 277 cctctccgag 10 278 10 DNA Homo sapiens 278 gggagtcatg 10 279 10 DNA Homo sapiens 279 gtggaagaag 10 280 10 DNA Homo sapiens 280 catgccttct 10 281 10 DNA Homo sapiens 281 ccgaaggtgg 10 282 10 DNA Homo sapiens 282 ctgcagcccc 10 283 10 DNA Homo sapiens 283 gggccgagac 10 284 10 DNA Homo sapiens 284 tcaggagttt 10 285 10 DNA Homo sapiens 285 accgcatgta 10 286 10 DNA Homo sapiens 286 aagcagctcc 10 287 10 DNA Homo sapiens 287 aggtgctctg 10 288 10 DNA Homo sapiens 288 tggagacagg 10 289 10 DNA Homo sapiens 289 gggggcgagg 10 290 10 DNA Homo sapiens 290 atcctgcccc 10 291 10 DNA Homo sapiens 291 gagcattgcc 10 292 10 DNA Homo sapiens 292 cttaggtgca 10 293 10 DNA Homo sapiens 293 acaagaggac 10 294 10 DNA Homo sapiens 294 taggtgcatg 10 295 10 DNA Homo sapiens 295 caacaagagg 10 296 10 DNA Homo sapiens 296 tagggcttat 10 297 10 DNA Homo sapiens 297 cccaggcatg 10 298 10 DNA Homo sapiens 298 ggcagccagg 10 299 10 DNA Homo sapiens 299 aaatctgcca 10 300 10 DNA Homo sapiens 300 catggcccac 10 301 10 DNA Homo sapiens 301 tgggcctcca 10 302 10 DNA Homo sapiens 302 aactaacaca 10 303 10 DNA Homo sapiens 303 cccttgatgg 10 304 10 DNA Homo sapiens 304 gagtaatgct 10 305 10 DNA Homo sapiens 305 acacacagac 10 306 10 DNA Homo sapiens 306 gaaacttgcc 10 307 10 DNA Homo sapiens 307 caaacccaga 10 308 22 DNA Homo sapiens 308 ccacagtcat cccgacacta gc 22 309 22 DNA Homo sapiens 309 tattccagcc gtatccatgt gc 22 310 22 DNA Homo sapiens 310 ccttggtgca tgtggtaaga gg 22 311 23 DNA Homo sapiens 311 tttcaaaggt gggaggactg agg 23 312 20 DNA Homo sapiens 312 gcagtgagct gggattgtgc 20 313 23 DNA Homo sapiens 313 aactcccctt ctctgatgtg agg 23 314 23 DNA Homo sapiens 314 tcacagttac agaggtggca agc 23 315 22 DNA Homo sapiens 315 ctgcctacct ggcagataca cc 22 316 22 DNA Homo sapiens 316 agctgtcact ccacctcctt gg 22 317 24 DNA Homo sapiens 317 aaagcctctg gtctgctaat gacc 24 318 22 DNA Homo sapiens 318 gggaggagat tcagagcact cc 22 319 22 DNA Homo sapiens 319 cagtccacgt ttccagaaca cc 22 320 21 DNA Homo sapiens 320 ggcttgggat aatggtgttg c 21 321 23 DNA Homo sapiens 321 tacttcccga aggtggaaga agg 23 322 24 DNA Homo sapiens 322 cagtggagat cagcaagaca gtcc 24 323 22 DNA Homo sapiens 323 gggcatctcg ggttctactt cc 22 324 23 DNA Homo sapiens 324 gggaagtacg agtgctcaca tgc 23 325 23 DNA Homo sapiens 325 cttatacccc tcttccccac tgc 23 326 21 DNA Homo sapiens 326 tctctgagcc aaccactgtg c 21 327 23 DNA Homo sapiens 327 ggctgagtag acaatgccac tgc 23 328 22 DNA Homo sapiens 328 ctgtgtcccc agagaaatgt gg 22 329 23 DNA Homo sapiens 329 gactcagcaa caagaggaca tgc 23 330 24 DNA Homo sapiens 330 ggcattgtct actcagccct tacc 24 331 20 DNA Homo sapiens 331 acaagtcgag gtgcccaagg 20 332 25 DNA Homo sapiens 332 cccacataca tgagggtctc ttagg 25 333 21 DNA Homo sapiens 333 attctgcctc cagcatcaac c 21 334 24 DNA Homo sapiens 334 aacagagctt ccttaggttg atgc 24 335 23 DNA Homo sapiens 335 cctcagttcc ccactacctt agc 23 336 18 DNA Homo sapiens 336 gcgctggccc tcaacttt 18 337 20 DNA Homo sapiens 337 gtccctggag atgggacctc 20 338 20 DNA Homo sapiens 338 gcccccagat ctgtcctcac 20 339 20 DNA Homo sapiens 339 ggaaaataca ggcggcttcc 20 340 22 DNA Homo sapiens 340 ggctctgaat ctgtgtggtg ct 22 341 20 DNA Homo sapiens 341 agccaggtga gaagccaggt 20 342 20 DNA Homo sapiens 342 ggcctgaaca ggacgaacaa 20 343 20 DNA Homo sapiens 343 ggcaggattg ccattagagg 20 344 22 DNA Homo sapiens 344 tgagtcagtg gtttgacctc ca 22 345 20 DNA Homo sapiens 345 gcctctgtct cccctgcaac 20 346 20 DNA Homo sapiens 346 ccacttttgc catcgaccac 20 347 20 DNA Homo sapiens 347 ctgccgtccc ttgaaggcta 20 348 22 DNA Homo sapiens 348 ccctaccctc agggatttct ca 22 349 20 DNA Homo sapiens 349 cccattctcc tctccgagca 20 350 20 DNA Homo sapiens 350 atcagcgtgg tgcgatgtgt 20 351 20 DNA Homo sapiens 351 acccagctct ctgggacacg 20 352 21 DNA Homo sapiens 352 gggatgagtt cccaagtgca g 21 353 20 DNA Homo sapiens 353 tggcaagcag gcttgagaag 20 354 20 DNA Homo sapiens 354 ccccaacctg agccagaaac 20 355 20 DNA Homo sapiens 355 tgtccacaag ggggtctgtg 20 356 20 DNA Homo sapiens 356 ggctagcagt ggggaagagg 20 357 18 DNA Homo sapiens 357 attgccaggg gcaggatg 18 358 20 DNA Homo sapiens 358 ccctgtcatg gccagtcctt 20 359 20 DNA Homo sapiens 359 gcgacccagt gccctctact 20 360 22 DNA Homo sapiens 360 tgcatgtcct cttgttgctg ag 22 361 20 DNA Homo sapiens 361 caatgaccac cctccctgaa 20 362 19 DNA Homo sapiens 362 cggctgtcaa ggggtgttc 19 363 20 DNA Homo sapiens 363 ccaaacccag acggcaagtt 20 364 24 DNA Homo sapiens 364 aaacccctgg actccaagtg atcc 24 365 24 DNA Homo sapiens 365 aagcgattct tctgcctcag cctc 24 366 24 DNA Homo sapiens 366 ggacagttgt tgtgtagctc accc 24 367 22 DNA Homo sapiens 367 ctatgttgcc caagctgacc tc 22 368 20 DNA Homo sapiens 368 gccctcaact ttgcctgcac 20 369 23 DNA Homo sapiens 369 agtccagtat tccagccgta tcc 23 370 22 DNA Homo sapiens 370 tgatcgggaa gctggaagag tc 22 371 22 DNA Homo sapiens 371 cgtttcaaag gtgggaggac tg 22 372 21 DNA Homo sapiens 372 cgaccaaaaa tctgggtggt g 21 373 21 DNA Homo sapiens 373 caggaagcaa agggacttgc c 21 374 22 DNA Homo sapiens 374 tcttaaacat ggtggggtca gc 22 375 21 DNA Homo sapiens 375 catggaaatt gtgggcttgt g 21 376 22 DNA Homo sapiens 376 atgtgcaaga gggagagtgg tg 22 377 22 DNA Homo sapiens 377 tgactgagag gactgcaaag gg 22 378 24 DNA Homo sapiens 378 gcctgatctc tgatgccaaa taag 24 379 20 DNA Homo sapiens 379 tttgccattc cagaagccag 20 380 23 DNA Homo sapiens 380 gatctgtgtg atgtcgaggc ttg 23 381 21 DNA Homo sapiens 381 gtccacgttt ccagaacacc c 21 382 22 DNA Homo sapiens 382 cgaaatccca aagacacaga cc 22 383 22 DNA Homo sapiens 383 gagttgctga agctgcggta ag 22 384 23 DNA Homo sapiens 384 gaaaaaggga gcttctgtgc atc 23 385 20 DNA Homo sapiens 385 aacaagggga cagggactgg 20 386 21 DNA Homo sapiens 386 cagaaacctg ggagcagatc c 21 387 24 DNA Homo sapiens 387 gcaacaagag gacatgcacc taag 24 388 23 DNA Homo sapiens 388 aaaggtagag gacatgccaa agc 23 389 21 DNA Homo sapiens 389 ggagcagcca acaactcgtt c 21 390 23 DNA Homo sapiens 390 gctcatttaa tccccacaac acc 23 391 23 DNA Homo sapiens 391 ccaccacacc tggctaattt ttg 23 392 23 DNA Homo sapiens 392 tgtagctcac cctctggact ttg 23 393 20 DNA Homo sapiens 393 aatatgcaac cctcccctgc 20 394 23 DNA Homo sapiens 394 tgaggcagaa gaatcgcttg aac 23 395 22 DNA Homo sapiens 395 acttgtcatt ggctgtcccc tc 22 396 21 DNA Homo sapiens 396 tttgcctgca ctgtgctttt g 21 397 23 DNA Homo sapiens 397 ccatactcag catcctgcac tcc 23 398 20 DNA Homo sapiens 398 aacgacagca accagggtgg 20 399 23 DNA Homo sapiens 399 cagcaggtgt atctaatggc agg 23 400 22 DNA Homo sapiens 400 agagtggtgg ggagatgagg tg 22 401 21 DNA Homo sapiens 401 tgcaaagggg cagactagag g 21 402 22 DNA Homo sapiens 402 cgaccacttt tatgggagga gc 22 403 23 DNA Homo sapiens 403 ccaggtgttc tgaaccacac ttc 23 404 23 DNA Homo sapiens 404 tgtgtgatgt cgaggcttgt acc 23 405 22 DNA Homo sapiens 405 gaatgcaggg aagagaaggc ag 22 406 22 DNA Homo sapiens 406 gccatcagga catggtgatt tc 22 407 22 DNA Homo sapiens 407 tgagcactcg tacttcccga ag 22 408 22 DNA Homo sapiens 408 tgagagcagc agggatgact tc 22 409 23 DNA Homo sapiens 409 aaactcctga tagccactgg tgg 23 410 20 DNA Homo sapiens 410 agatcctccg ccgaaatgtc 20 411 24 DNA Homo sapiens 411 ttactcttct ctgagatgcc cgag 24 412 22 DNA Homo sapiens 412 tgggcagtgg cattgtctac tc 22 413 20 DNA Homo sapiens 413 ttccaggagg tggcatttcc 20 

What is claimed is:
 1. An isolated polynucleotide comprising a nucleotide sequence selected from the group consisting of: (a) a first nucleotide sequence which is a polymorphic variant of a reference sequence for Interleukin 4 Receptor Alpha(IL4Rα) gene or a fragment thereof, wherein the reference sequence comprises SEQ ID NO:1, and the polymorphic variant comprises an IL4Rα isogene defined by a haplotype selected from the group consisting of haplotypes 1-53 in Table 5; and (b) a second nucleotide sequence which is complementary to the first nucleotide sequence.
 3. The isolated polynucleotide of claim 1 which is a DNA molecule and comprises both the first and second nucleotide sequences and further comprises expression regulatory elements operably linked to the first nucleotide sequence.
 4. A recombinant organism transformed or transfected with the isolated polynucleotide of claim 1, wherein the organism expresses an IL4Rα protein encoded by the first nucleotide sequence.
 5. The recombinant organism of claim 4 which is a nonhuman transgenic animal.
 6. The isolated polynucleotide of claim 1, wherein the first nucleotide sequence is a polymorphic variant of a fragment of the IL4Rα isogene, the fragment comprising one or more polymorphisms selected from the group consisting of: guanine at PS1, thymine at PS2, thymine at PS3, cytosine at PS4, thymine at PS6, adenine at PS7, cytosine at PS8, thymine at PS9, thymine at PS10, adenine at PS11, adenine at PS12, thymine at PS13, thymine at PS14, adenine at PS15, thymine at PS16, adenine at PS17, thymine at PS18, adenine at PS19, cytosine at PS20, cytosine at PS21, thymine at PS22, cytosine at PS23, thymine at PS25, thymine at PS27, cytosine at PS28, thymine at PS30, adenine at PS32, thymine at PS33, guanine at PS34, cytosine at PS35, cytosine at PS36, cytosine at PS37, thymine at PS38, guanine at PS39, guanine at PS40, adenine at PS41, thymine at PS44, and adenine at PS45.
 7. An isolated polynucleotide comprising a nucleotide sequence which is a polymorphic variant of a reference sequence for the IL4Rα cDNA or a fragment thereof, wherein the reference sequence comprises SEQ ID NO:2 and the polymorphic variant comprises adenine or guanine at a position corresponding to nucleotide 223, cytosine or thymine at a position corresponding to nucleotide 237, guanine or adenine at a position corresponding to nucleotide 244, thymine or cytosine at a position corresponding to nucleotide 291, cytosine or thymine at a position corresponding to nucleotide 501, guanine or adenine at a position corresponding to nucleotide 554, thymine or cytosine at a position corresponding to nucleotide 939, adenine or cytosine at a position corresponding to nucleotide 1198, guanine or thymine at a position corresponding to nucleotide 1242, thymine or cytosine at a position corresponding to nucleotide 1291, cytosine or thymine at a position corresponding to nucleotide 1293, thymine or cytosine at a position corresponding to nucleotide 1299, thymine or cytosine at a position corresponding to nucleotide 1507, cytosine or thymine at a position corresponding to nucleotide 1701, adenine or guanine at a position corresponding to nucleotide 1727, guanine or adenine at a position corresponding to nucleotide 1735, cytosine or thymine at a position corresponding to nucleotide 2023, thynine or guanine at a position corresponding to nucleotide 2254 and thymine or cytosine at a position corresponding to nucleotide
 2397. 8. A recombinant organism transformed or transfected with the isolated polynucleotide of claim 7, wherein the organism expresses a Interleukin 4 Receptor Alpha(IL4Rα) protein encoded by the polymorphic variant sequence.
 9. The recombinant organism of claim 8 which is a nonhuman transgenic animal.
 10. An isolated polypeptide comprising an amino acid sequence which is a polymorphic variant of a reference sequence for the IL4Rα protein or a fragment thereof, wherein the reference sequence comprises SEQ ID NO: 3 and the polymorphic variant is encoded by an isogene defined by one of the haplotypes shown in Table
 5. 11. An isolated antibody specific for and immunoreactive with the isolated polypeptide of claim
 10. 12. A method for screening for drugs targeting the isolated polypeptide of claim 10 which comprises contacting the IL4Rα polymorphic variant with a candidate agent and assaying for binding activity.
 13. A composition comprising at least one genotyping oligonucleotide for detecting a polymorphism in the Interleukin 4 Receptor Alpha(IL4Rα) gene at a polymorphic site selected from PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18,PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45.
 14. The composition of claim 13, wherein the genotyping oligonucleotide is an allele-specific oligonucleotide that specifically hybridizes to an allele of the IL4Rα gene at a region containing the polymorphic site.
 15. The composition of claim 14, wherein the allele-specific oligonucleotide comprises a nucleotide sequence selected from the group consisting of of SEQ ID NOS:4-79, the complements of SEQ ID NOS: 4-79, and SEQ ID NOS:80-231.
 16. The composition of claim 13, wherein the genotyping oligonucleotide is a primer-extension oligonucleotide.
 17. A method for genotyping the Interleukin 4 Receptor Alpha(IL4Rα) gene of an individual, comprising determining for the two copies of the IL4Rα gene present in the individual the identity of the nucleotide pair at each of PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45.
 18. The method of claim 17, wherein the determining step comprises: (a) isolating from the individual a nucleic acid mixture comprising both copies of the IL4Rα gene, or a fragment thereof, that are present in the individual; (b) amplifying from the nucleic acid mixture a target region containing at least one of the polymorphic sites; (c) hybridizing a primer extension oligonucleotide to one allele of the amplified target region; (d) performing a nucleic acid template-dependent, primer extension reaction on the hybridized genotyping oligonucleotide in the presence of at least two different terminators of the reaction, wherein said terminators are complementary to the alternative nucleotides present at the polymorphic site; and (e) detecting the presence and identity of the terminator in the extended genotyping oligonucleotide.
 19. A method for haplotyping the Interleukin 4 Receptor Alpha(IL4Rα) gene of an individual which comprises determining, for one copy of the IL4Rα gene present in the individual, the identity of the nucleotide at each of PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45.
 20. The method of claim 19, wherein the determining step comprises (a) isolating from the individual a nucleic acid molecule containing only one of the two copies of the IL4Rα gene, or a fragment thereof, that is present in the individual; (b) amplifying from the nucleic acid molecule a target region containing at least one of the polymorphic sites; (c) hybridizing a primer extension oligonucleotide to one allele of the amplified target region; (d) performing a nucleic acid template-dependent, primer extension reaction on the hybridized genotyping oligonucleotide in the presence of at least two different terminators of the reaction, wherein said terminators are complementary to the alternative nucleotides present at the polymorphic site; and (e) detecting the presence and identity of the terminator in the extended genotyping oligonucleotide.
 21. A method for predicting a haplotype pair for the Interleukin 4 Receptor Alpha(IL4Rα) gene of an individual comprising: (a) identifying an IL4Rα genotype for the individual at each of PS1, PS2, PS3, PS4, PS6, PS7, PS8, PS9, PS10, PS11, PS12, PS13, PS14, PS15, PS16, PS17, PS18, PS19, PS20, PS21, PS22, PS23, PS25, PS27, PS28, PS30, PS32, PS33, PS34, PS35, PS36, PS37, PS38, PS39, PS40, PS41, PS44, and PS45; (b) enumerating all possible haplotype pairs which are consistent with the genotype; (c) accessing data containing the IL4Rα haplotype pairs determined in a reference population; and (d) assigning a haplotype pair to the individual that is consistent with the data.
 22. A method for identifying an association between a trait and at least one haplotype of the Interleukin 4 Receptor Alpha gene which comprises comparing the frequency of the haplotype in a population exhibiting the trait with the frequency of the haplotype in a reference population, wherein the haplotype is selected from haplotype numbers 1-53 shown in Table 5, wherein a higher frequency of the haplotype in the trait population than in the reference population indicates the trait is associated with the haplotype.
 24. The method of claim 22, wherein the trait is a clinical response to a drug targeting IL4Rα.
 25. A computer system for storing and analyzing polymorphism data for the Interleukin 4 Receptor Alphagene, comprising: (a) a central processing unit (CPU); (b) a communication interface; (c) a display device; (d) an input device; and (e) a database containing the polymorphism data; wherein the polymorphism data comprises the genotypes and haplotype pairs shown in Table 4 and the haplotypes shown in Table
 5. 26. A genome anthology for the Interleukin 4 Receptor Alpha(IL4Rα) gene which comprises IL4Rα isogenes defined by haplotypes 1-53 shown in Table
 5. 27. A method for haplotyping the Interleukin 4 Receptor Alpha(IL4Rα) gene of an individual which comprises determining whether the individual has one or more haplotypes in Table
 5. 